Canonical Allele Identifier: CA2677797197

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945411-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945411T>G , CM000668.2:g.29945411T>G	GRCh38
NC_000006.11:g.29913188T>G , CM000668.1:g.29913188T>G	GRCh37
NC_000006.10:g.30021167T>G	NCBI36
NG_029217.2:g.7947T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.977-40T>G	ENSP00000492789.2:n.977-40T>G
ENST00000706892.1:n.2763T>G
ENST00000706893.1:c.*78-40T>G	ENSP00000516609.1:n.*78-40T>G
ENST00000706894.1:c.*38T>G	ENSP00000516610.1:n.*38T>G
ENST00000706895.1:n.2043T>G
ENST00000706896.1:n.2390-40T>G
ENST00000706897.1:n.1812-40T>G
ENST00000706898.1:c.1112-40T>G	ENSP00000516611.1:n.1112-40T>G
ENST00000706899.1:n.1948-40T>G
ENST00000706900.1:c.1010-40T>G	ENSP00000516617.1:n.1010-40T>G
ENST00000706901.1:c.1094-40T>G	ENSP00000516612.1:n.1094-40T>G
ENST00000706902.1:c.1093+130T>G	ENSP00000516613.1:n.1093+130T>G
ENST00000706903.1:c.1094-40T>G	ENSP00000516614.1:n.1094-40T>G
ENST00000706904.1:c.1093+130T>G	ENSP00000516615.1:n.1093+130T>G
ENST00000706905.1:c.1094-40T>G	ENSP00000516616.1:n.1094-40T>G
ENST00000376809.10:c.1094-40T>G MANE Select	ENSP00000366005.5:n.1094-40T>G
ENST00000376802.2:c.896-40T>G	ENSP00000365998.2:n.896-40T>G
ENST00000376806.9:c.1112-40T>G	ENSP00000366002.5:n.1112-40T>G
ENST00000376809.9:c.1094-40T>G	ENSP00000366005.5:n.1094-40T>G
ENST00000396634.5:c.1094-40T>G	ENSP00000379873.1:n.1094-40T>G
ENST00000495183.5:n.1333-40T>G
ENST00000496081.5:n.1353-40T>G
NM_002116.7:c.1094-40T>G	NP_002107.3:n.1094-40T>G
NM_002116.8:c.1094-40T>G MANE Select	NP_002107.3:n.1094-40T>G