Canonical Allele Identifier: CA1619077188
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268952G= , CM000668.2:g.31268952G= GRCh38
NC_000006.11:g.31236729G= , CM000668.1:g.31236729G= GRCh37
NC_000006.10:g.31344708G= NCBI36
NG_029422.2:g.8180C=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*217C= MANE Select ENSP00000365402.5:n.*217C=
ENST00000376228.9:c.*217C= ENSP00000365402.5:n.*217C=
ENST00000376237.8:c.*905C= ENSP00000365412.4:n.*905C=
ENST00000383329.7:c.*217C= ENSP00000372819.3:n.*217C=
ENST00000466892.5:n.551C=
ENST00000470363.5:n.1076C=
ENST00000487245.5:n.1677C=
NM_002117.5:c.*217C= NP_002108.4:n.*217C=
NM_002117.6:c.*217C= MANE Select NP_002108.4:n.*217C=