Canonical Allele Identifier: CA2641148026
Gene: MC2R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13885327_13885329del , CM000680.2:g.13885327_13885329del GRCh38
NC_000018.9:g.13885326_13885328del , CM000680.1:g.13885326_13885328del GRCh37
NC_000018.8:g.13875326_13875328del NCBI36
NG_011819.1:g.35208_35210del

Transcript Alleles

HGVS Amino-acid Change
ENST00000327606.4:c.190_192del MANE Select ENSP00000333821.2:p.Cys64del
ENST00000327606.3:c.190_192del ENSP00000333821.2:p.Cys64del
ENST00000399821.2:c.190_192del ENSP00000382718.2:p.Cys64del
NM_000529.2:c.190_192del MANE Select NP_000520.1:p.Cys64del
NM_001291911.1:c.190_192del NP_001278840.1:p.Cys64del
XM_017025781.1:c.190_192del XP_016881270.1:p.Cys64del