Canonical Allele Identifier: CA2677798480

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945755-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945757del , CM000668.2:g.29945757del	GRCh38
NC_000006.11:g.29913534del , CM000668.1:g.29913534del	GRCh37
NC_000006.10:g.30021513del	NCBI36
NG_029217.2:g.8293del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1283del	ENSP00000492789.2:n.1283del
ENST00000706895.1:n.2389del
ENST00000706896.1:n.2696del
ENST00000706897.1:n.2118del
ENST00000706898.1:c.*302del	ENSP00000516611.1:n.*302del
ENST00000706899.1:n.2254del
ENST00000706900.1:c.*302del	ENSP00000516617.1:n.*302del
ENST00000706901.1:c.*302del	ENSP00000516612.1:n.*302del
ENST00000706902.1:c.1093+476del	ENSP00000516613.1:n.1093+476del
ENST00000706903.1:c.*124+178del	ENSP00000516614.1:n.*124+178del
ENST00000706904.1:c.1093+476del	ENSP00000516615.1:n.1093+476del
ENST00000706905.1:c.*302del	ENSP00000516616.1:n.*302del
ENST00000376809.10:c.*302del MANE Select	ENSP00000366005.5:n.*302del
ENST00000376802.2:c.*302del	ENSP00000365998.2:n.*302del
ENST00000376806.9:c.*302del	ENSP00000366002.5:n.*302del
ENST00000376809.9:c.*302del	ENSP00000366005.5:n.*302del
ENST00000396634.5:c.*302del	ENSP00000379873.1:n.*302del
ENST00000495183.5:n.1639del
ENST00000496081.5:n.1659del
NM_002116.7:c.*302del	NP_002107.3:n.*302del
NM_002116.8:c.*302del MANE Select	NP_002107.3:n.*302del