Canonical Allele Identifier: CA823770013

Gene: HLA-A

Linked Data

• dbSNP Id: rs1386913013
• gnomAD v3: 6-29945857-G-A
• gnomAD v4: 6-29945857-G-A
• MyVariant Identifiers: chr6:g.29913634G>A (hg19) ; chr6:g.29945857G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945857G>A , CM000668.2:g.29945857G>A	GRCh38
NC_000006.11:g.29913634G>A , CM000668.1:g.29913634G>A	GRCh37
NC_000006.10:g.30021613G>A	NCBI36
NG_029217.2:g.8393G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1383G>A	ENSP00000492789.2:n.1383G>A
ENST00000706899.1:n.2354G>A
ENST00000706900.1:c.*402G>A	ENSP00000516617.1:n.*402G>A
ENST00000706901.1:c.*402G>A	ENSP00000516612.1:n.*402G>A
ENST00000706902.1:c.1093+576G>A	ENSP00000516613.1:n.1093+576G>A
ENST00000706903.1:c.*124+278G>A	ENSP00000516614.1:n.*124+278G>A
ENST00000706904.1:c.1093+576G>A	ENSP00000516615.1:n.1093+576G>A
ENST00000706905.1:c.*402G>A	ENSP00000516616.1:n.*402G>A
ENST00000376809.10:c.*402G>A MANE Select	ENSP00000366005.5:n.*402G>A
ENST00000376802.2:c.*402G>A	ENSP00000365998.2:n.*402G>A
ENST00000376806.9:c.*402G>A	ENSP00000366002.5:n.*402G>A
ENST00000376809.9:c.*402G>A	ENSP00000366005.5:n.*402G>A
ENST00000396634.5:c.*402G>A	ENSP00000379873.1:n.*402G>A
ENST00000495183.5:n.1739G>A
ENST00000496081.5:n.1759G>A
NM_002116.7:c.*402G>A	NP_002107.3:n.*402G>A
NM_002116.8:c.*402G>A MANE Select	NP_002107.3:n.*402G>A