Canonical Allele Identifier: CA2285919218
Gene: MC2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884688_13884692delinsGGCAT , CM000680.2:g.13884688_13884692delinsGGCAT GRCh38
NC_000018.9:g.13884687_13884691delinsGGCAT , CM000680.1:g.13884687_13884691delinsGGCAT GRCh37
NC_000018.8:g.13874687_13874691delinsGGCAT NCBI36
NG_011819.1:g.35845_35849delinsATGCC

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.827_831delinsATGCC MANE Select ENSP00000333821.2:p.Tyr276=
ENST00000327606.3:c.827_831delinsATGCC ENSP00000333821.2:p.Tyr276=
NM_000529.2:c.827_831delinsATGCC MANE Select NP_000520.1:p.Tyr276=
NM_001291911.1:c.827_831delinsATGCC NP_001278840.1:p.Tyr276=
XM_017025781.1:c.827_831delinsATGCC XP_016881270.1:p.Tyr276=