Canonical Allele Identifier: CA565893700

Gene: HLA-A

Linked Data

• dbSNP Id: rs1157312752
• gnomAD v2: 6-29913349-G-A
• gnomAD v3: 6-29945572-G-A
• gnomAD v4: 6-29945572-G-A
• MyVariant Identifiers: chr6:g.29913349G>A (hg19) ; chr6:g.29945572G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945572G>A , CM000668.2:g.29945572G>A	GRCh38
NC_000006.11:g.29913349G>A , CM000668.1:g.29913349G>A	GRCh37
NC_000006.10:g.30021328G>A	NCBI36
NG_029217.2:g.8108G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1098G>A	ENSP00000492789.2:n.1098G>A
ENST00000706892.1:n.2924G>A
ENST00000706893.1:c.*199G>A	ENSP00000516609.1:n.*199G>A
ENST00000706894.1:c.*199G>A	ENSP00000516610.1:n.*199G>A
ENST00000706895.1:n.2204G>A
ENST00000706896.1:n.2511G>A
ENST00000706897.1:n.1933G>A
ENST00000706898.1:c.*117G>A	ENSP00000516611.1:n.*117G>A
ENST00000706899.1:n.2069G>A
ENST00000706900.1:c.*117G>A	ENSP00000516617.1:n.*117G>A
ENST00000706901.1:c.*117G>A	ENSP00000516612.1:n.*117G>A
ENST00000706902.1:c.1093+291G>A	ENSP00000516613.1:n.1093+291G>A
ENST00000706903.1:c.*117G>A	ENSP00000516614.1:n.*117G>A
ENST00000706904.1:c.1093+291G>A	ENSP00000516615.1:n.1093+291G>A
ENST00000706905.1:c.*117G>A	ENSP00000516616.1:n.*117G>A
ENST00000376809.10:c.*117G>A MANE Select	ENSP00000366005.5:n.*117G>A
ENST00000376802.2:c.*117G>A	ENSP00000365998.2:n.*117G>A
ENST00000376806.9:c.*117G>A	ENSP00000366002.5:n.*117G>A
ENST00000376809.9:c.*117G>A	ENSP00000366005.5:n.*117G>A
ENST00000396634.5:c.*117G>A	ENSP00000379873.1:n.*117G>A
ENST00000495183.5:n.1454G>A
ENST00000496081.5:n.1474G>A
NM_002116.7:c.*117G>A	NP_002107.3:n.*117G>A
NM_002116.8:c.*117G>A MANE Select	NP_002107.3:n.*117G>A