Canonical Allele Identifier: CA2677797219

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945413-ATG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945414_29945415del , CM000668.2:g.29945414_29945415del	GRCh38
NC_000006.11:g.29913191_29913192del , CM000668.1:g.29913191_29913192del	GRCh37
NC_000006.10:g.30021170_30021171del	NCBI36
NG_029217.2:g.7950_7951del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.977-37_977-36del	ENSP00000492789.2:n.977-37_977-36del
ENST00000706892.1:n.2766_2767del
ENST00000706893.1:c.*78-37_*78-36del	ENSP00000516609.1:n.*78-37_*78-36del
ENST00000706894.1:c.*41_*42del	ENSP00000516610.1:n.*41_*42del
ENST00000706895.1:n.2046_2047del
ENST00000706896.1:n.2390-37_2390-36del
ENST00000706897.1:n.1812-37_1812-36del
ENST00000706898.1:c.1112-37_1112-36del	ENSP00000516611.1:n.1112-37_1112-36del
ENST00000706899.1:n.1948-37_1948-36del
ENST00000706900.1:c.1010-37_1010-36del	ENSP00000516617.1:n.1010-37_1010-36del
ENST00000706901.1:c.1094-37_1094-36del	ENSP00000516612.1:n.1094-37_1094-36del
ENST00000706902.1:c.1093+133_1093+134del	ENSP00000516613.1:n.1093+133_1093+134del
ENST00000706903.1:c.1094-37_1094-36del	ENSP00000516614.1:n.1094-37_1094-36del
ENST00000706904.1:c.1093+133_1093+134del	ENSP00000516615.1:n.1093+133_1093+134del
ENST00000706905.1:c.1094-37_1094-36del	ENSP00000516616.1:n.1094-37_1094-36del
ENST00000376809.10:c.1094-37_1094-36del MANE Select	ENSP00000366005.5:n.1094-37_1094-36del
ENST00000376802.2:c.896-37_896-36del	ENSP00000365998.2:n.896-37_896-36del
ENST00000376806.9:c.1112-37_1112-36del	ENSP00000366002.5:n.1112-37_1112-36del
ENST00000376809.9:c.1094-37_1094-36del	ENSP00000366005.5:n.1094-37_1094-36del
ENST00000396634.5:c.1094-37_1094-36del	ENSP00000379873.1:n.1094-37_1094-36del
ENST00000495183.5:n.1333-37_1333-36del
ENST00000496081.5:n.1353-37_1353-36del
NM_002116.7:c.1094-37_1094-36del	NP_002107.3:n.1094-37_1094-36del
NM_002116.8:c.1094-37_1094-36del MANE Select	NP_002107.3:n.1094-37_1094-36del