Canonical Allele Identifier: CA2677794526

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29943003-GCTA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29943008_29943010del , CM000668.2:g.29943008_29943010del	GRCh38
NC_000006.11:g.29910785_29910787del , CM000668.1:g.29910785_29910787del	GRCh37
NC_000006.10:g.30018764_30018766del	NCBI36
NG_029217.2:g.5543_5545del

Transcript Alleles

HGVS	Amino-acid change
ENST00000638375.2:c.325_327del	ENSP00000492789.2:p.Tyr109del
ENST00000706892.1:n.601_603del
ENST00000706893.1:c.325_327del	ENSP00000516609.1:p.Tyr109del
ENST00000706894.1:c.325_327del	ENSP00000516610.1:p.Tyr109del
ENST00000706895.1:n.601_603del
ENST00000706896.1:n.601_603del
ENST00000706897.1:n.601_603del
ENST00000706898.1:c.325_327del	ENSP00000516611.1:p.Tyr109del
ENST00000706899.1:n.601_603del
ENST00000706900.1:c.241_243del	ENSP00000516617.1:p.Tyr81del
ENST00000706901.1:c.325_327del	ENSP00000516612.1:p.Tyr109del
ENST00000706902.1:c.325_327del	ENSP00000516613.1:p.Tyr109del
ENST00000706903.1:c.325_327del	ENSP00000516614.1:p.Tyr109del
ENST00000706904.1:c.325_327del	ENSP00000516615.1:p.Tyr109del
ENST00000706905.1:c.325_327del	ENSP00000516616.1:p.Tyr109del
ENST00000376809.10:c.325_327del MANE Select	ENSP00000366005.5:p.Tyr109del
ENST00000638375.1:c.325_327del	ENSP00000492789.1:p.Tyr109del
ENST00000376802.2:c.325_327del	ENSP00000365998.2:p.Tyr109del
ENST00000376806.9:c.325_327del	ENSP00000366002.5:p.Tyr109del
ENST00000376809.9:c.325_327del	ENSP00000366005.5:p.Tyr109del
ENST00000396634.5:c.325_327del	ENSP00000379873.1:p.Tyr109del
ENST00000429656.1:n.62_64del
ENST00000461903.1:n.325_327del
ENST00000479320.5:n.325_327del
ENST00000495183.5:n.327_329del
ENST00000496081.5:n.177+154_177+156del
NM_002116.7:c.325_327del	NP_002107.3:p.Tyr109del
NM_002116.8:c.325_327del MANE Select	NP_002107.3:p.Tyr109del