Canonical Allele Identifier: CA1619080434
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271228C= , CM000668.2:g.31271228C= GRCh38
NC_000006.11:g.31239005C= , CM000668.1:g.31239005C= GRCh37
NC_000006.10:g.31346984C= NCBI36
NG_029422.2:g.5904G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.464G= MANE Select ENSP00000365402.5:p.Arg155=
ENST00000376228.9:c.464G= ENSP00000365402.5:p.Arg155=
ENST00000376237.8:c.*51G= ENSP00000365412.4:n.*51G=
ENST00000383329.7:c.464G= ENSP00000372819.3:p.Arg155=
ENST00000415537.1:c.462G=
ENST00000484378.1:n.733G=
ENST00000487245.5:n.823G=
ENST00000495835.1:n.653G=
NM_002117.5:c.464G= NP_002108.4:p.Arg155=
NM_002117.6:c.464G= MANE Select NP_002108.4:p.Arg155=