Canonical Allele Identifier: CA2677797971

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945611-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945611T>A , CM000668.2:g.29945611T>A	GRCh38
NC_000006.11:g.29913388T>A , CM000668.1:g.29913388T>A	GRCh37
NC_000006.10:g.30021367T>A	NCBI36
NG_029217.2:g.8147T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1137T>A	ENSP00000492789.2:n.1137T>A
ENST00000706892.1:n.2963T>A
ENST00000706893.1:c.*238T>A	ENSP00000516609.1:n.*238T>A
ENST00000706894.1:c.*238T>A	ENSP00000516610.1:n.*238T>A
ENST00000706895.1:n.2243T>A
ENST00000706896.1:n.2550T>A
ENST00000706897.1:n.1972T>A
ENST00000706898.1:c.*156T>A	ENSP00000516611.1:n.*156T>A
ENST00000706899.1:n.2108T>A
ENST00000706900.1:c.*156T>A	ENSP00000516617.1:n.*156T>A
ENST00000706901.1:c.*156T>A	ENSP00000516612.1:n.*156T>A
ENST00000706902.1:c.1093+330T>A	ENSP00000516613.1:n.1093+330T>A
ENST00000706903.1:c.*124+32T>A	ENSP00000516614.1:n.*124+32T>A
ENST00000706904.1:c.1093+330T>A	ENSP00000516615.1:n.1093+330T>A
ENST00000706905.1:c.*156T>A	ENSP00000516616.1:n.*156T>A
ENST00000376809.10:c.*156T>A MANE Select	ENSP00000366005.5:n.*156T>A
ENST00000376802.2:c.*156T>A	ENSP00000365998.2:n.*156T>A
ENST00000376806.9:c.*156T>A	ENSP00000366002.5:n.*156T>A
ENST00000376809.9:c.*156T>A	ENSP00000366005.5:n.*156T>A
ENST00000396634.5:c.*156T>A	ENSP00000379873.1:n.*156T>A
ENST00000495183.5:n.1493T>A
ENST00000496081.5:n.1513T>A
NM_002116.7:c.*156T>A	NP_002107.3:n.*156T>A
NM_002116.8:c.*156T>A MANE Select	NP_002107.3:n.*156T>A