Canonical Allele Identifier: CA2285919168
Gene: MC2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884603_13884604delinsCT , CM000680.2:g.13884603_13884604delinsCT GRCh38
NC_000018.9:g.13884602_13884603delinsCT , CM000680.1:g.13884602_13884603delinsCT GRCh37
NC_000018.8:g.13874602_13874603delinsCT NCBI36
NG_011819.1:g.35933_35934delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.*21_*22delinsAG MANE Select ENSP00000333821.2:n.*21_*22delinsAG
ENST00000327606.3:c.*21_*22delinsAG ENSP00000333821.2:n.*21_*22delinsAG
NM_000529.2:c.*21_*22delinsAG MANE Select NP_000520.1:n.*21_*22delinsAG
NM_001291911.1:c.*21_*22delinsAG NP_001278840.1:n.*21_*22delinsAG
XM_017025781.1:c.*21_*22delinsAG XP_016881270.1:n.*21_*22delinsAG