Canonical Allele Identifier: CA1619080355
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271145A= , CM000668.2:g.31271145A= GRCh38
NC_000006.11:g.31238922A= , CM000668.1:g.31238922A= GRCh37
NC_000006.10:g.31346901A= NCBI36
NG_029422.2:g.5987T=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.547T= MANE Select ENSP00000365402.5:p.Tyr183=
ENST00000376228.9:c.547T= ENSP00000365402.5:p.Tyr183=
ENST00000376237.8:c.*134T= ENSP00000365412.4:n.*134T=
ENST00000383329.7:c.547T= ENSP00000372819.3:p.Tyr183=
ENST00000415537.1:c.545T=
ENST00000484378.1:n.816T=
ENST00000487245.5:n.906T=
ENST00000495835.1:n.736T=
NM_002117.5:c.547T= NP_002108.4:p.Tyr183=
NM_002117.6:c.547T= MANE Select NP_002108.4:p.Tyr183=