Canonical Allele Identifier: CA3693457

Gene: HLA-A

Linked Data

• dbSNP Id: rs556330213
• ExAC: 6:29911333 A / G
• gnomAD v2: 6-29911333-A-G
• gnomAD v3: 6-29943556-A-G
• gnomAD v4: 6-29943556-A-G
• MyVariant Identifiers: chr6:g.29911333A>G (hg19) ; chr6:g.29943556A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29943556A>G , CM000668.2:g.29943556A>G	GRCh38
NC_000006.11:g.29911333A>G , CM000668.1:g.29911333A>G	GRCh37
NC_000006.10:g.30019312A>G	NCBI36
NG_029217.2:g.6091A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.619+13A>G	ENSP00000492789.2:n.619+13A>G
ENST00000706892.1:n.908A>G
ENST00000706893.1:c.619+13A>G	ENSP00000516609.1:n.619+13A>G
ENST00000706894.1:c.619+13A>G	ENSP00000516610.1:n.619+13A>G
ENST00000706895.1:n.895+13A>G
ENST00000706896.1:n.908A>G
ENST00000706897.1:n.895+13A>G
ENST00000706898.1:c.619+13A>G	ENSP00000516611.1:n.619+13A>G
ENST00000706899.1:n.908A>G
ENST00000706900.1:c.535+13A>G	ENSP00000516617.1:n.535+13A>G
ENST00000706901.1:c.619+13A>G	ENSP00000516612.1:n.619+13A>G
ENST00000706902.1:c.619+13A>G	ENSP00000516613.1:n.619+13A>G
ENST00000706903.1:c.619+13A>G	ENSP00000516614.1:n.619+13A>G
ENST00000706904.1:c.619+13A>G	ENSP00000516615.1:n.619+13A>G
ENST00000706905.1:c.619+13A>G	ENSP00000516616.1:n.619+13A>G
ENST00000376809.10:c.619+13A>G MANE Select	ENSP00000366005.5:n.619+13A>G
ENST00000638375.1:c.619+13A>G	ENSP00000492789.1:n.619+13A>G
ENST00000376802.2:c.619+13A>G	ENSP00000365998.2:n.619+13A>G
ENST00000376806.9:c.619+13A>G	ENSP00000366002.5:n.619+13A>G
ENST00000376809.9:c.619+13A>G	ENSP00000366005.5:n.619+13A>G
ENST00000396634.5:c.619+13A>G	ENSP00000379873.1:n.619+13A>G
ENST00000461903.1:n.860+13A>G
ENST00000479320.5:n.860+13A>G
ENST00000495183.5:n.862+13A>G
ENST00000496081.5:n.436+13A>G
NM_002116.7:c.619+13A>G	NP_002107.3:n.619+13A>G
NM_002116.8:c.619+13A>G MANE Select	NP_002107.3:n.619+13A>G