Canonical Allele Identifier: CA1619077248
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269050G= , CM000668.2:g.31269050G= GRCh38
NC_000006.11:g.31236827G= , CM000668.1:g.31236827G= GRCh37
NC_000006.10:g.31344806G= NCBI36
NG_029422.2:g.8082C=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*119C= MANE Select ENSP00000365402.5:n.*119C=
ENST00000376228.9:c.*119C= ENSP00000365402.5:n.*119C=
ENST00000376237.8:c.*807C= ENSP00000365412.4:n.*807C=
ENST00000383329.7:c.*119C= ENSP00000372819.3:n.*119C=
ENST00000466892.5:n.453C=
ENST00000470363.5:n.978C=
ENST00000487245.5:n.1579C=
NM_002117.5:c.*119C= NP_002108.4:n.*119C=
NM_002117.6:c.*119C= MANE Select NP_002108.4:n.*119C=