Canonical Allele Identifier: CA2677951429

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31271393-C-CCCCGCCCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271393_31271394insCCCGCCCCA , CM000668.2:g.31271393_31271394insCCCGCCCCA	GRCh38
NC_000006.11:g.31239170_31239171insCCCGCCCCA , CM000668.1:g.31239170_31239171insCCCGCCCCA	GRCh37
NC_000006.10:g.31347149_31347150insCCCGCCCCA	NCBI36
NG_029422.2:g.5738_5739insTGGGGCGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.344-46_344-45insTGGGGCGGG MANE Select	ENSP00000365402.5:n.344-46_344-45insTGGGGCGGG
ENST00000376228.9:c.344-46_344-45insTGGGGCGGG	ENSP00000365402.5:n.344-46_344-45insTGGGGCGGG
ENST00000376237.8:c.344-63_344-62insTGGGGCGGG	ENSP00000365412.4:n.344-63_344-62insTGGGGCGGG
ENST00000383329.7:c.344-46_344-45insTGGGGCGGG	ENSP00000372819.3:n.344-46_344-45insTGGGGCGGG
ENST00000415537.1:c.342-46_342-45insTGGGGCGGG
ENST00000484378.1:n.567_568insTGGGGCGGG
ENST00000487245.5:n.657_658insTGGGGCGGG
ENST00000495835.1:n.533-46_533-45insTGGGGCGGG
NM_002117.5:c.344-46_344-45insTGGGGCGGG	NP_002108.4:n.344-46_344-45insTGGGGCGGG
NM_002117.6:c.344-46_344-45insTGGGGCGGG MANE Select	NP_002108.4:n.344-46_344-45insTGGGGCGGG