Canonical Allele Identifier: CA2578557188

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29944191-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944194del , CM000668.2:g.29944194del	GRCh38
NC_000006.11:g.29911971del , CM000668.1:g.29911971del	GRCh37
NC_000006.10:g.30019950del	NCBI36
NG_029217.2:g.6730del

Transcript Alleles

HGVS	Amino-acid change
ENST00000638375.2:c.692del	ENSP00000492789.2:p.Gly231AlafsTer9
ENST00000706892.1:n.1546del
ENST00000706893.1:c.692del	ENSP00000516609.1:p.Gly231AlafsTer9
ENST00000706894.1:c.692del	ENSP00000516610.1:p.Gly231AlafsTer9
ENST00000706895.1:n.968del
ENST00000706896.1:n.1546del
ENST00000706897.1:n.968del
ENST00000706898.1:c.692del	ENSP00000516611.1:p.Gly231AlafsTer9
ENST00000706899.1:n.1546del
ENST00000706900.1:c.608del	ENSP00000516617.1:p.Gly203AlafsTer9
ENST00000706901.1:c.692del	ENSP00000516612.1:p.Gly231AlafsTer9
ENST00000706902.1:c.692del	ENSP00000516613.1:p.Gly231AlafsTer9
ENST00000706903.1:c.692del	ENSP00000516614.1:p.Gly231AlafsTer9
ENST00000706904.1:c.692del	ENSP00000516615.1:p.Gly231AlafsTer9
ENST00000706905.1:c.692del	ENSP00000516616.1:p.Gly231AlafsTer9
ENST00000376809.10:c.692del MANE Select	ENSP00000366005.5:p.Gly231AlafsTer9
ENST00000638375.1:c.692del	ENSP00000492789.1:p.Gly231AlafsTer9
ENST00000376802.2:c.692del	ENSP00000365998.2:p.Gly231AlafsTer9
ENST00000376806.9:c.692del	ENSP00000366002.5:p.Gly231AlafsTer9
ENST00000376809.9:c.692del	ENSP00000366005.5:p.Gly231AlafsTer9
ENST00000396634.5:c.692del	ENSP00000379873.1:p.Gly231AlafsTer9
ENST00000461903.1:n.933del
ENST00000479320.5:n.933del
ENST00000495183.5:n.935del
ENST00000496081.5:n.509del
NM_002116.7:c.692del	NP_002107.3:p.Gly231AlafsTer9
NM_002116.8:c.692del MANE Select	NP_002107.3:p.Gly231AlafsTer9