Canonical Allele Identifier: CA3693745

Gene: HLA-A

Linked Data

• dbSNP Id: rs41546815
• ExAC: 6:29913078 A / G
• gnomAD v2: 6-29913078-A-G
• gnomAD v3: 6-29945301-A-G
• gnomAD v4: 6-29945301-A-G
• MyVariant Identifiers: chr6:g.29913078A>G (hg19) ; chr6:g.29945301A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945301A>G , CM000668.2:g.29945301A>G	GRCh38
NC_000006.11:g.29913078A>G , CM000668.1:g.29913078A>G	GRCh37
NC_000006.10:g.30021057A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.976+20A>G	ENSP00000492789.2:n.976+20A>G
ENST00000706892.1:n.2653A>G
ENST00000706893.1:c.*77+20A>G	ENSP00000516609.1:n.*77+20A>G
ENST00000706894.1:c.1113A>G	ENSP00000516610.1:p.Leu371=
ENST00000706895.1:n.1933A>G
ENST00000706896.1:n.2389+20A>G
ENST00000706897.1:n.1811+20A>G
ENST00000706898.1:c.1111+20A>G	ENSP00000516611.1:n.1111+20A>G
ENST00000706899.1:n.1947+20A>G
ENST00000706900.1:c.1009+20A>G	ENSP00000516617.1:n.1009+20A>G
ENST00000706901.1:c.1093+20A>G	ENSP00000516612.1:n.1093+20A>G
ENST00000706902.1:c.1093+20A>G	ENSP00000516613.1:n.1093+20A>G
ENST00000706903.1:c.1093+20A>G	ENSP00000516614.1:n.1093+20A>G
ENST00000706904.1:c.1093+20A>G	ENSP00000516615.1:n.1093+20A>G
ENST00000706905.1:c.1093+20A>G	ENSP00000516616.1:n.1093+20A>G
ENST00000376809.10:c.1093+20A>G MANE Select	ENSP00000366005.5:n.1093+20A>G
ENST00000376802.2:c.896-150A>G	ENSP00000365998.2:n.896-150A>G
ENST00000376806.9:c.1111+20A>G	ENSP00000366002.5:n.1111+20A>G
ENST00000376809.9:c.1093+20A>G	ENSP00000366005.5:n.1093+20A>G
ENST00000396634.5:c.1093+20A>G	ENSP00000379873.1:n.1093+20A>G
ENST00000495183.5:n.1332+20A>G
ENST00000496081.5:n.1352+20A>G
NM_002116.7:c.1093+20A>G	NP_002107.3:n.1093+20A>G
NM_002116.8:c.1093+20A>G MANE Select	NP_002107.3:n.1093+20A>G