Canonical Allele Identifier: CA1619080437
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271231A= , CM000668.2:g.31271231A= GRCh38
NC_000006.11:g.31239008A= , CM000668.1:g.31239008A= GRCh37
NC_000006.10:g.31346987A= NCBI36
NG_029422.2:g.5901T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.461T= MANE Select ENSP00000365402.5:p.Leu154=
ENST00000376228.9:c.461T= ENSP00000365402.5:p.Leu154=
ENST00000376237.8:c.*48T= ENSP00000365412.4:n.*48T=
ENST00000383329.7:c.461T= ENSP00000372819.3:p.Leu154=
ENST00000415537.1:c.459T=
ENST00000484378.1:n.730T=
ENST00000487245.5:n.820T=
ENST00000495835.1:n.650T=
NM_002117.5:c.461T= NP_002108.4:p.Leu154=
NM_002117.6:c.461T= MANE Select NP_002108.4:p.Leu154=