Canonical Allele Identifier: CA1619077321
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269091G= , CM000668.2:g.31269091G= GRCh38
NC_000006.11:g.31236868G= , CM000668.1:g.31236868G= GRCh37
NC_000006.10:g.31344847G= NCBI36
NG_029422.2:g.8041C=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*78C= MANE Select ENSP00000365402.5:n.*78C=
ENST00000376228.9:c.*78C= ENSP00000365402.5:n.*78C=
ENST00000376237.8:c.*766C= ENSP00000365412.4:n.*766C=
ENST00000383329.7:c.*78C= ENSP00000372819.3:n.*78C=
ENST00000466892.5:n.412C=
ENST00000470363.5:n.937C=
ENST00000487245.5:n.1538C=
NM_002117.5:c.*78C= NP_002108.4:n.*78C=
NM_002117.6:c.*78C= MANE Select NP_002108.4:n.*78C=