Canonical Allele Identifier: CA363326600
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31271268-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271268A>T , CM000668.2:g.31271268A>T GRCh38
NC_000006.11:g.31239045A>T , CM000668.1:g.31239045A>T GRCh37
NC_000006.10:g.31347024A>T NCBI36
NG_029422.2:g.5864T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.424T>A MANE Select ENSP00000365402.5:p.Tyr142Asn
ENST00000376228.9:c.424T>A ENSP00000365402.5:p.Tyr142Asn
ENST00000376237.8:c.*11T>A ENSP00000365412.4:n.*11T>A
ENST00000383329.7:c.424T>A ENSP00000372819.3:p.Tyr142Asn
ENST00000415537.1:c.422T>A
ENST00000484378.1:n.693T>A
ENST00000487245.5:n.783T>A
ENST00000495835.1:n.613T>A
NM_002117.5:c.424T>A NP_002108.4:p.Tyr142Asn
NM_002117.6:c.424T>A MANE Select NP_002108.4:p.Tyr142Asn