Canonical Allele Identifier: CA2285919155
Gene: MC2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884578_13884579delinsCT , CM000680.2:g.13884578_13884579delinsCT GRCh38
NC_000018.9:g.13884577_13884578delinsCT , CM000680.1:g.13884577_13884578delinsCT GRCh37
NC_000018.8:g.13874577_13874578delinsCT NCBI36
NG_011819.1:g.35958_35959delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.*46_*47delinsAG MANE Select ENSP00000333821.2:n.*46_*47delinsAG
ENST00000327606.3:c.*46_*47delinsAG ENSP00000333821.2:n.*46_*47delinsAG
NM_000529.2:c.*46_*47delinsAG MANE Select NP_000520.1:n.*46_*47delinsAG
NM_001291911.1:c.*46_*47delinsAG NP_001278840.1:n.*46_*47delinsAG
XM_017025781.1:c.*46_*47delinsAG XP_016881270.1:n.*46_*47delinsAG