Canonical Allele Identifier: CA2677950306
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270014dup , CM000668.2:g.31270014dup GRCh38
NC_000006.11:g.31237791dup , CM000668.1:g.31237791dup GRCh37
NC_000006.10:g.31345770dup NCBI36
NG_029422.2:g.7118dup

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.967dup MANE Select ENSP00000365402.5:p.Val323GlyfsTer12
ENST00000376228.9:c.967dup ENSP00000365402.5:p.Val323GlyfsTer12
ENST00000376237.8:c.*554dup ENSP00000365412.4:n.*554dup
ENST00000383329.7:c.967dup ENSP00000372819.3:p.Val323GlyfsTer12
ENST00000470363.5:n.285dup
ENST00000487245.5:n.1326dup
NM_002117.5:c.967dup NP_002108.4:p.Val323GlyfsTer12
NM_002117.6:c.967dup MANE Select NP_002108.4:p.Val323GlyfsTer12