Canonical Allele Identifier: CA1619080319
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271114C= , CM000668.2:g.31271114C= GRCh38
NC_000006.11:g.31238891C= , CM000668.1:g.31238891C= GRCh37
NC_000006.10:g.31346870C= NCBI36
NG_029422.2:g.6018G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.578G= MANE Select ENSP00000365402.5:p.Arg193=
ENST00000376228.9:c.578G= ENSP00000365402.5:p.Arg193=
ENST00000376237.8:c.*165G= ENSP00000365412.4:n.*165G=
ENST00000383329.7:c.578G= ENSP00000372819.3:p.Arg193=
ENST00000415537.1:c.576G=
ENST00000484378.1:n.847G=
ENST00000487245.5:n.937G=
ENST00000495835.1:n.767G=
NM_002117.5:c.578G= NP_002108.4:p.Arg193=
NM_002117.6:c.578G= MANE Select NP_002108.4:p.Arg193=