Canonical Allele Identifier: CA2677797991

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945620-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945620T>G , CM000668.2:g.29945620T>G	GRCh38
NC_000006.11:g.29913397T>G , CM000668.1:g.29913397T>G	GRCh37
NC_000006.10:g.30021376T>G	NCBI36
NG_029217.2:g.8156T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1146T>G	ENSP00000492789.2:n.1146T>G
ENST00000706892.1:n.2972T>G
ENST00000706893.1:c.*247T>G	ENSP00000516609.1:n.*247T>G
ENST00000706894.1:c.*247T>G	ENSP00000516610.1:n.*247T>G
ENST00000706895.1:n.2252T>G
ENST00000706896.1:n.2559T>G
ENST00000706897.1:n.1981T>G
ENST00000706898.1:c.*165T>G	ENSP00000516611.1:n.*165T>G
ENST00000706899.1:n.2117T>G
ENST00000706900.1:c.*165T>G	ENSP00000516617.1:n.*165T>G
ENST00000706901.1:c.*165T>G	ENSP00000516612.1:n.*165T>G
ENST00000706902.1:c.1093+339T>G	ENSP00000516613.1:n.1093+339T>G
ENST00000706903.1:c.*124+41T>G	ENSP00000516614.1:n.*124+41T>G
ENST00000706904.1:c.1093+339T>G	ENSP00000516615.1:n.1093+339T>G
ENST00000706905.1:c.*165T>G	ENSP00000516616.1:n.*165T>G
ENST00000376809.10:c.*165T>G MANE Select	ENSP00000366005.5:n.*165T>G
ENST00000376802.2:c.*165T>G	ENSP00000365998.2:n.*165T>G
ENST00000376806.9:c.*165T>G	ENSP00000366002.5:n.*165T>G
ENST00000376809.9:c.*165T>G	ENSP00000366005.5:n.*165T>G
ENST00000396634.5:c.*165T>G	ENSP00000379873.1:n.*165T>G
ENST00000495183.5:n.1502T>G
ENST00000496081.5:n.1522T>G
NM_002116.7:c.*165T>G	NP_002107.3:n.*165T>G
NM_002116.8:c.*165T>G MANE Select	NP_002107.3:n.*165T>G