Canonical Allele Identifier: CA2677951361

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31271350-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271352del , CM000668.2:g.31271352del	GRCh38
NC_000006.11:g.31239129del , CM000668.1:g.31239129del	GRCh37
NC_000006.10:g.31347108del	NCBI36
NG_029422.2:g.5781del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.344-3del MANE Select	ENSP00000365402.5:n.344-3del
ENST00000376228.9:c.344-3del	ENSP00000365402.5:n.344-3del
ENST00000376237.8:c.344-20del	ENSP00000365412.4:n.344-20del
ENST00000383329.7:c.344-3del	ENSP00000372819.3:n.344-3del
ENST00000415537.1:c.342-3del
ENST00000484378.1:n.610del
ENST00000487245.5:n.700del
ENST00000495835.1:n.533-3del
NM_002117.5:c.344-3del	NP_002108.4:n.344-3del
NM_002117.6:c.344-3del MANE Select	NP_002108.4:n.344-3del