Canonical Allele Identifier: CA1619077225
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269016G= , CM000668.2:g.31269016G= GRCh38
NC_000006.11:g.31236793G= , CM000668.1:g.31236793G= GRCh37
NC_000006.10:g.31344772G= NCBI36
NG_029422.2:g.8116C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*153C= MANE Select ENSP00000365402.5:n.*153C=
ENST00000376228.9:c.*153C= ENSP00000365402.5:n.*153C=
ENST00000376237.8:c.*841C= ENSP00000365412.4:n.*841C=
ENST00000383329.7:c.*153C= ENSP00000372819.3:n.*153C=
ENST00000466892.5:n.487C=
ENST00000470363.5:n.1012C=
ENST00000487245.5:n.1613C=
NM_002117.5:c.*153C= NP_002108.4:n.*153C=
NM_002117.6:c.*153C= MANE Select NP_002108.4:n.*153C=