Canonical Allele Identifier: CA363326475

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31271259-T-A
• MyVariant Identifiers: chr6:g.31239036T>A (hg19) ; chr6:g.31271259T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271259T>A , CM000668.2:g.31271259T>A	GRCh38
NC_000006.11:g.31239036T>A , CM000668.1:g.31239036T>A	GRCh37
NC_000006.10:g.31347015T>A	NCBI36
NG_029422.2:g.5873A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.433A>T MANE Select	ENSP00000365402.5:p.Lys145Ter
ENST00000376228.9:c.433A>T	ENSP00000365402.5:p.Lys145Ter
ENST00000376237.8:c.*20A>T	ENSP00000365412.4:n.*20A>T
ENST00000383329.7:c.433A>T	ENSP00000372819.3:p.Lys145Ter
ENST00000415537.1:c.431A>T
ENST00000484378.1:n.702A>T
ENST00000487245.5:n.792A>T
ENST00000495835.1:n.622A>T
NM_002117.5:c.433A>T	NP_002108.4:p.Lys145Ter
NM_002117.6:c.433A>T MANE Select	NP_002108.4:p.Lys145Ter