Canonical Allele Identifier: CA2677798105

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29945671-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945673del , CM000668.2:g.29945673del	GRCh38
NC_000006.11:g.29913450del , CM000668.1:g.29913450del	GRCh37
NC_000006.10:g.30021429del	NCBI36
NG_029217.2:g.8209del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1199del	ENSP00000492789.2:n.1199del
ENST00000706892.1:n.3025del
ENST00000706893.1:c.*300del	ENSP00000516609.1:n.*300del
ENST00000706894.1:c.*300del	ENSP00000516610.1:n.*300del
ENST00000706895.1:n.2305del
ENST00000706896.1:n.2612del
ENST00000706897.1:n.2034del
ENST00000706898.1:c.*218del	ENSP00000516611.1:n.*218del
ENST00000706899.1:n.2170del
ENST00000706900.1:c.*218del	ENSP00000516617.1:n.*218del
ENST00000706901.1:c.*218del	ENSP00000516612.1:n.*218del
ENST00000706902.1:c.1093+392del	ENSP00000516613.1:n.1093+392del
ENST00000706903.1:c.*124+94del	ENSP00000516614.1:n.*124+94del
ENST00000706904.1:c.1093+392del	ENSP00000516615.1:n.1093+392del
ENST00000706905.1:c.*218del	ENSP00000516616.1:n.*218del
ENST00000376809.10:c.*218del MANE Select	ENSP00000366005.5:n.*218del
ENST00000376802.2:c.*218del	ENSP00000365998.2:n.*218del
ENST00000376806.9:c.*218del	ENSP00000366002.5:n.*218del
ENST00000376809.9:c.*218del	ENSP00000366005.5:n.*218del
ENST00000396634.5:c.*218del	ENSP00000379873.1:n.*218del
ENST00000495183.5:n.1555del
ENST00000496081.5:n.1575del
NM_002116.7:c.*218del	NP_002107.3:n.*218del
NM_002116.8:c.*218del MANE Select	NP_002107.3:n.*218del