Canonical Allele Identifier: CA363319601
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269998A>T , CM000668.2:g.31269998A>T GRCh38
NC_000006.11:g.31237775A>T , CM000668.1:g.31237775A>T GRCh37
NC_000006.10:g.31345754A>T NCBI36
NG_029422.2:g.7134T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.983T>A MANE Select ENSP00000365402.5:p.Val328Asp
ENST00000376228.9:c.983T>A ENSP00000365402.5:p.Val328Asp
ENST00000376237.8:c.*570T>A ENSP00000365412.4:n.*570T>A
ENST00000383329.7:c.983T>A ENSP00000372819.3:p.Val328Asp
ENST00000470363.5:n.301T>A
ENST00000487245.5:n.1342T>A
NM_002117.5:c.983T>A NP_002108.4:p.Val328Asp
NM_002117.6:c.983T>A MANE Select NP_002108.4:p.Val328Asp