Canonical Allele Identifier: CA1619080478
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271280C= , CM000668.2:g.31271280C= GRCh38
NC_000006.11:g.31239057C= , CM000668.1:g.31239057C= GRCh37
NC_000006.10:g.31347036C= NCBI36
NG_029422.2:g.5852G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.412G= MANE Select ENSP00000365402.5:p.Asp138=
ENST00000376228.9:c.412G= ENSP00000365402.5:p.Asp138=
ENST00000376237.8:c.395G= ENSP00000365412.4:p.Ter132=
ENST00000383329.7:c.412G= ENSP00000372819.3:p.Asp138=
ENST00000415537.1:c.410G=
ENST00000484378.1:n.681G=
ENST00000487245.5:n.771G=
ENST00000495835.1:n.601G=
NM_002117.5:c.412G= NP_002108.4:p.Asp138=
NM_002117.6:c.412G= MANE Select NP_002108.4:p.Asp138=