Canonical Allele Identifier: CA823770000

Gene: HLA-A

Linked Data

• dbSNP Id: rs1443507957
• gnomAD v3: 6-29945822-G-A
• gnomAD v4: 6-29945822-G-A
• MyVariant Identifiers: chr6:g.29913599G>A (hg19) ; chr6:g.29945822G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945822G>A , CM000668.2:g.29945822G>A	GRCh38
NC_000006.11:g.29913599G>A , CM000668.1:g.29913599G>A	GRCh37
NC_000006.10:g.30021578G>A	NCBI36
NG_029217.2:g.8358G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1348G>A	ENSP00000492789.2:n.1348G>A
ENST00000706896.1:n.2761G>A
ENST00000706897.1:n.2183G>A
ENST00000706898.1:c.*367G>A	ENSP00000516611.1:n.*367G>A
ENST00000706899.1:n.2319G>A
ENST00000706900.1:c.*367G>A	ENSP00000516617.1:n.*367G>A
ENST00000706901.1:c.*367G>A	ENSP00000516612.1:n.*367G>A
ENST00000706902.1:c.1093+541G>A	ENSP00000516613.1:n.1093+541G>A
ENST00000706903.1:c.*124+243G>A	ENSP00000516614.1:n.*124+243G>A
ENST00000706904.1:c.1093+541G>A	ENSP00000516615.1:n.1093+541G>A
ENST00000706905.1:c.*367G>A	ENSP00000516616.1:n.*367G>A
ENST00000376809.10:c.*367G>A MANE Select	ENSP00000366005.5:n.*367G>A
ENST00000376802.2:c.*367G>A	ENSP00000365998.2:n.*367G>A
ENST00000376806.9:c.*367G>A	ENSP00000366002.5:n.*367G>A
ENST00000376809.9:c.*367G>A	ENSP00000366005.5:n.*367G>A
ENST00000396634.5:c.*367G>A	ENSP00000379873.1:n.*367G>A
ENST00000495183.5:n.1704G>A
ENST00000496081.5:n.1724G>A
NM_002116.7:c.*367G>A	NP_002107.3:n.*367G>A
NM_002116.8:c.*367G>A MANE Select	NP_002107.3:n.*367G>A