Canonical Allele Identifier: CA1619079934
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270437G= , CM000668.2:g.31270437G= GRCh38
NC_000006.11:g.31238214G= , CM000668.1:g.31238214G= GRCh37
NC_000006.10:g.31346193G= NCBI36
NG_029422.2:g.6695C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.668C= MANE Select ENSP00000365402.5:p.Ala223=
ENST00000376228.9:c.668C= ENSP00000365402.5:p.Ala223=
ENST00000376237.8:c.*255C= ENSP00000365412.4:n.*255C=
ENST00000383329.7:c.668C= ENSP00000372819.3:p.Ala223=
ENST00000415537.1:c.664+2C=
ENST00000487245.5:n.1027C=
ENST00000495835.1:n.857C=
NM_002117.5:c.668C= NP_002108.4:p.Ala223=
NM_002117.6:c.668C= MANE Select NP_002108.4:p.Ala223=