Canonical Allele Identifier: CA565893687

Gene: HLA-A

Linked Data

• dbSNP Id: rs1561766580
• gnomAD v2: 6-29913200-A-G
• gnomAD v3: 6-29945423-A-G
• gnomAD v4: 6-29945423-A-G
• MyVariant Identifiers: chr6:g.29913200_29913215delinsGTTTGTTCATGAATAT (hg19) ; chr6:g.29945423_29945438delinsGTTTGTTCATGAATAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945423A>G , CM000668.2:g.29945423A>G	GRCh38
NC_000006.11:g.29913200A>G , CM000668.1:g.29913200A>G	GRCh37
NC_000006.10:g.30021179A>G	NCBI36
NG_029217.2:g.7959A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.977-28A>G	ENSP00000492789.2:n.977-28A>G
ENST00000706892.1:n.2775A>G
ENST00000706893.1:c.*78-28A>G	ENSP00000516609.1:n.*78-28A>G
ENST00000706894.1:c.*50A>G	ENSP00000516610.1:n.*50A>G
ENST00000706895.1:n.2055A>G
ENST00000706896.1:n.2390-28A>G
ENST00000706897.1:n.1812-28A>G
ENST00000706898.1:c.1112-28A>G	ENSP00000516611.1:n.1112-28A>G
ENST00000706899.1:n.1948-28A>G
ENST00000706900.1:c.1010-28A>G	ENSP00000516617.1:n.1010-28A>G
ENST00000706901.1:c.1094-28A>G	ENSP00000516612.1:n.1094-28A>G
ENST00000706902.1:c.1093+142A>G	ENSP00000516613.1:n.1093+142A>G
ENST00000706903.1:c.1094-28A>G	ENSP00000516614.1:n.1094-28A>G
ENST00000706904.1:c.1093+142A>G	ENSP00000516615.1:n.1093+142A>G
ENST00000706905.1:c.1094-28A>G	ENSP00000516616.1:n.1094-28A>G
ENST00000376809.10:c.1094-28A>G MANE Select	ENSP00000366005.5:n.1094-28A>G
ENST00000376802.2:c.896-28A>G	ENSP00000365998.2:n.896-28A>G
ENST00000376806.9:c.1112-28A>G	ENSP00000366002.5:n.1112-28A>G
ENST00000376809.9:c.1094-28A>G	ENSP00000366005.5:n.1094-28A>G
ENST00000396634.5:c.1094-28A>G	ENSP00000379873.1:n.1094-28A>G
ENST00000495183.5:n.1333-28A>G
ENST00000496081.5:n.1353-28A>G
NM_002116.7:c.1094-28A>G	NP_002107.3:n.1094-28A>G
NM_002116.8:c.1094-28A>G MANE Select	NP_002107.3:n.1094-28A>G