Canonical Allele Identifier: CA136025459

Gene: HLA-A

Linked Data

• dbSNP Id: rs45603432
• MyVariant Identifiers: chr6:g.29912715del (hg19) ; chr6:g.29944938del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944940del , CM000668.2:g.29944940del	GRCh38
NC_000006.11:g.29912717del , CM000668.1:g.29912717del	GRCh37
NC_000006.10:g.30020696del	NCBI36
NG_029217.2:g.7476del

Transcript Alleles

HGVS	Amino-acid change
ENST00000638375.2:c.896-119del	ENSP00000492789.2:n.896-119del
ENST00000706892.1:n.2292del
ENST00000706893.1:c.1065-119del	ENSP00000516609.1:n.1065-119del
ENST00000706894.1:c.1013-119del	ENSP00000516610.1:n.1013-119del
ENST00000706895.1:n.1714del
ENST00000706896.1:n.2190del
ENST00000706897.1:n.1612del
ENST00000706898.1:c.1031-119del	ENSP00000516611.1:n.1031-119del
ENST00000706899.1:n.1867-119del
ENST00000706900.1:c.929-119del	ENSP00000516617.1:n.929-119del
ENST00000706901.1:c.1013-119del	ENSP00000516612.1:n.1013-119del
ENST00000706902.1:c.1013-119del	ENSP00000516613.1:n.1013-119del
ENST00000706903.1:c.1013-119del	ENSP00000516614.1:n.1013-119del
ENST00000706904.1:c.1013-119del	ENSP00000516615.1:n.1013-119del
ENST00000706905.1:c.1013-119del	ENSP00000516616.1:n.1013-119del
ENST00000376809.10:c.1013-119del MANE Select	ENSP00000366005.5:n.1013-119del
ENST00000638375.1:c.896-119del	ENSP00000492789.1:n.896-119del
ENST00000376802.2:c.896-511del	ENSP00000365998.2:n.896-511del
ENST00000376806.9:c.1031-119del	ENSP00000366002.5:n.1031-119del
ENST00000376809.9:c.1013-119del	ENSP00000366005.5:n.1013-119del
ENST00000396634.5:c.1013-119del	ENSP00000379873.1:n.1013-119del
ENST00000461903.1:n.1272-119del
ENST00000479320.5:n.1254-119del
ENST00000495183.5:n.1256-123del
ENST00000496081.5:n.1153del
NM_002116.7:c.1013-119del	NP_002107.3:n.1013-119del
NM_002116.8:c.1013-119del MANE Select	NP_002107.3:n.1013-119del