Canonical Allele Identifier: CA2677951398

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31271373-CAGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271374_31271376del , CM000668.2:g.31271374_31271376del	GRCh38
NC_000006.11:g.31239151_31239153del , CM000668.1:g.31239151_31239153del	GRCh37
NC_000006.10:g.31347130_31347132del	NCBI36
NG_029422.2:g.5756_5758del

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.344-28_344-26del MANE Select	ENSP00000365402.5:n.344-28_344-26del
ENST00000376228.9:c.344-28_344-26del	ENSP00000365402.5:n.344-28_344-26del
ENST00000376237.8:c.344-45_344-43del	ENSP00000365412.4:n.344-45_344-43del
ENST00000383329.7:c.344-28_344-26del	ENSP00000372819.3:n.344-28_344-26del
ENST00000415537.1:c.342-28_342-26del
ENST00000484378.1:n.585_587del
ENST00000487245.5:n.675_677del
ENST00000495835.1:n.533-28_533-26del
NM_002117.5:c.344-28_344-26del	NP_002108.4:n.344-28_344-26del
NM_002117.6:c.344-28_344-26del MANE Select	NP_002108.4:n.344-28_344-26del