Assay Details
Target Gene Details
Entrez Gene ID: | 4162 |
Gene Name: | melanoma cell adhesion molecule |
Gene Aliases: |
CD146, MUC18 |
Location: |
Chr.11:119308524-119317132 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 12 - Exon 13 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
MCAM | NM_006500.2 | NP_006491.2 | ||
XM_017017759.1 | XP_016873248.1 | |||
XM_017017760.1 | XP_016873249.1 | |||
XM_017017761.1 | XP_016873250.1 | |||
XM_017017762.1 | XP_016873251.1 | |||
AB209925.1 | BAD93162.1 | |||
AF089868.1 | AAD17799.1 | |||
AK126303.1 | BAC86520.1 | |||
AK128335.1 | 12 | 1707 | ||
AK291571.1 | ||||
AK312430.1 | ||||
BC056418.1 | AAH56418.1 | |||
M28882.1 | AAA20922.1 | |||
M29277.1 | AAA20824.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv952747 | Chr.11:119308591 - 119317490 on Build GRCh38 | Deletion | MIR6756 MCAM |
nsv556469 | Chr.11:119308968 - 119314637 on Build GRCh38 | Gain | MIR6756 MCAM |
More Information
Additional Information:
For this assay, SNP(s) [rs370970803] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic Non-exonic DGV Variation |