Canonical Allele Identifier: CA2677796650

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945291-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945293del , CM000668.2:g.29945293del	GRCh38
NC_000006.11:g.29913070del , CM000668.1:g.29913070del	GRCh37
NC_000006.10:g.30021049del	NCBI36
NG_029217.2:g.7829del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.976+12del	ENSP00000492789.2:n.976+12del
ENST00000706892.1:n.2645del
ENST00000706893.1:c.*77+12del	ENSP00000516609.1:n.*77+12del
ENST00000706894.1:c.1105del	ENSP00000516610.1:p.Glu369ArgfsTer3
ENST00000706895.1:n.1925del
ENST00000706896.1:n.2389+12del
ENST00000706897.1:n.1811+12del
ENST00000706898.1:c.1111+12del	ENSP00000516611.1:n.1111+12del
ENST00000706899.1:n.1947+12del
ENST00000706900.1:c.1009+12del	ENSP00000516617.1:n.1009+12del
ENST00000706901.1:c.1093+12del	ENSP00000516612.1:n.1093+12del
ENST00000706902.1:c.1093+12del	ENSP00000516613.1:n.1093+12del
ENST00000706903.1:c.1093+12del	ENSP00000516614.1:n.1093+12del
ENST00000706904.1:c.1093+12del	ENSP00000516615.1:n.1093+12del
ENST00000706905.1:c.1093+12del	ENSP00000516616.1:n.1093+12del
ENST00000376809.10:c.1093+12del MANE Select	ENSP00000366005.5:n.1093+12del
ENST00000376802.2:c.896-158del	ENSP00000365998.2:n.896-158del
ENST00000376806.9:c.1111+12del	ENSP00000366002.5:n.1111+12del
ENST00000376809.9:c.1093+12del	ENSP00000366005.5:n.1093+12del
ENST00000396634.5:c.1093+12del	ENSP00000379873.1:n.1093+12del
ENST00000495183.5:n.1332+12del
ENST00000496081.5:n.1352+12del
NM_002116.7:c.1093+12del	NP_002107.3:n.1093+12del
NM_002116.8:c.1093+12del MANE Select	NP_002107.3:n.1093+12del