Canonical Allele Identifier: CA2677797814

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945560-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945560T>G , CM000668.2:g.29945560T>G	GRCh38
NC_000006.11:g.29913337T>G , CM000668.1:g.29913337T>G	GRCh37
NC_000006.10:g.30021316T>G	NCBI36
NG_029217.2:g.8096T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000638375.2:c.1086T>G	ENSP00000492789.2:n.1086T>G
ENST00000706892.1:n.2912T>G
ENST00000706893.1:c.*187T>G	ENSP00000516609.1:n.*187T>G
ENST00000706894.1:c.*187T>G	ENSP00000516610.1:n.*187T>G
ENST00000706895.1:n.2192T>G
ENST00000706896.1:n.2499T>G
ENST00000706897.1:n.1921T>G
ENST00000706898.1:c.*105T>G	ENSP00000516611.1:n.*105T>G
ENST00000706899.1:n.2057T>G
ENST00000706900.1:c.*105T>G	ENSP00000516617.1:n.*105T>G
ENST00000706901.1:c.*105T>G	ENSP00000516612.1:n.*105T>G
ENST00000706902.1:c.1093+279T>G	ENSP00000516613.1:n.1093+279T>G
ENST00000706903.1:c.*105T>G	ENSP00000516614.1:n.*105T>G
ENST00000706904.1:c.1093+279T>G	ENSP00000516615.1:n.1093+279T>G
ENST00000706905.1:c.*105T>G	ENSP00000516616.1:n.*105T>G
ENST00000376809.10:c.*105T>G MANE Select	ENSP00000366005.5:n.*105T>G
ENST00000376802.2:c.*105T>G	ENSP00000365998.2:n.*105T>G
ENST00000376806.9:c.*105T>G	ENSP00000366002.5:n.*105T>G
ENST00000376809.9:c.*105T>G	ENSP00000366005.5:n.*105T>G
ENST00000396634.5:c.*105T>G	ENSP00000379873.1:n.*105T>G
ENST00000495183.5:n.1442T>G
ENST00000496081.5:n.1462T>G
NM_002116.7:c.*105T>G	NP_002107.3:n.*105T>G
NM_002116.8:c.*105T>G MANE Select	NP_002107.3:n.*105T>G