Canonical Allele Identifier: CA136025929

Gene: HLA-A

Linked Data

• dbSNP Id: rs763522908
• gnomAD v4: 6-29945595-G-A
• MyVariant Identifiers: chr6:g.29913372G>A (hg19) ; chr6:g.29945595G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945595G>A , CM000668.2:g.29945595G>A	GRCh38
NC_000006.11:g.29913372G>A , CM000668.1:g.29913372G>A	GRCh37
NC_000006.10:g.30021351G>A	NCBI36
NG_029217.2:g.8131G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1121G>A	ENSP00000492789.2:n.1121G>A
ENST00000706892.1:n.2947G>A
ENST00000706893.1:c.*222G>A	ENSP00000516609.1:n.*222G>A
ENST00000706894.1:c.*222G>A	ENSP00000516610.1:n.*222G>A
ENST00000706895.1:n.2227G>A
ENST00000706896.1:n.2534G>A
ENST00000706897.1:n.1956G>A
ENST00000706898.1:c.*140G>A	ENSP00000516611.1:n.*140G>A
ENST00000706899.1:n.2092G>A
ENST00000706900.1:c.*140G>A	ENSP00000516617.1:n.*140G>A
ENST00000706901.1:c.*140G>A	ENSP00000516612.1:n.*140G>A
ENST00000706902.1:c.1093+314G>A	ENSP00000516613.1:n.1093+314G>A
ENST00000706903.1:c.*124+16G>A	ENSP00000516614.1:n.*124+16G>A
ENST00000706904.1:c.1093+314G>A	ENSP00000516615.1:n.1093+314G>A
ENST00000706905.1:c.*140G>A	ENSP00000516616.1:n.*140G>A
ENST00000376809.10:c.*140G>A MANE Select	ENSP00000366005.5:n.*140G>A
ENST00000376802.2:c.*140G>A	ENSP00000365998.2:n.*140G>A
ENST00000376806.9:c.*140G>A	ENSP00000366002.5:n.*140G>A
ENST00000376809.9:c.*140G>A	ENSP00000366005.5:n.*140G>A
ENST00000396634.5:c.*140G>A	ENSP00000379873.1:n.*140G>A
ENST00000495183.5:n.1477G>A
ENST00000496081.5:n.1497G>A
NM_002116.7:c.*140G>A	NP_002107.3:n.*140G>A
NM_002116.8:c.*140G>A MANE Select	NP_002107.3:n.*140G>A