Canonical Allele Identifier: CA823769142

Gene: HLA-A

Linked Data

• dbSNP Id: rs1429530138
• MyVariant Identifiers: chr6:g.29912402_29912403del (hg19) ; chr6:g.29944625_29944626del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944627_29944628del , CM000668.2:g.29944627_29944628del	GRCh38
NC_000006.11:g.29912404_29912405del , CM000668.1:g.29912404_29912405del	GRCh37
NC_000006.10:g.30020383_30020384del	NCBI36
NG_029217.2:g.7163_7164del

Transcript Alleles

HGVS	Amino-acid change
ENST00000638375.2:c.895+230_895+231del	ENSP00000492789.2:n.895+230_895+231del
ENST00000706892.1:n.1979_1980del
ENST00000706893.1:c.1057_1058del	ENSP00000516609.1:p.Gly353Ter
ENST00000706894.1:c.1012+11_1012+12del	ENSP00000516610.1:n.1012+11_1012+12del
ENST00000706895.1:n.1401_1402del
ENST00000706896.1:n.1877_1878del
ENST00000706897.1:n.1299_1300del
ENST00000706898.1:c.1023_1024del	ENSP00000516611.1:p.Val342GlufsTer3
ENST00000706899.1:n.1866+11_1866+12del
ENST00000706900.1:c.928+11_928+12del	ENSP00000516617.1:n.928+11_928+12del
ENST00000706901.1:c.1012+11_1012+12del	ENSP00000516612.1:n.1012+11_1012+12del
ENST00000706902.1:c.1012+11_1012+12del	ENSP00000516613.1:n.1012+11_1012+12del
ENST00000706903.1:c.1012+11_1012+12del	ENSP00000516614.1:n.1012+11_1012+12del
ENST00000706904.1:c.1012+11_1012+12del	ENSP00000516615.1:n.1012+11_1012+12del
ENST00000706905.1:c.1012+11_1012+12del	ENSP00000516616.1:n.1012+11_1012+12del
ENST00000376809.10:c.1012+11_1012+12del MANE Select	ENSP00000366005.5:n.1012+11_1012+12del
ENST00000638375.1:c.895+230_895+231del	ENSP00000492789.1:n.895+230_895+231del
ENST00000376802.2:c.895+230_895+231del	ENSP00000365998.2:n.895+230_895+231del
ENST00000376806.9:c.1023_1024del	ENSP00000366002.5:p.Val342GlufsTer3
ENST00000376809.9:c.1012+11_1012+12del	ENSP00000366005.5:n.1012+11_1012+12del
ENST00000396634.5:c.1012+11_1012+12del	ENSP00000379873.1:n.1012+11_1012+12del
ENST00000461903.1:n.1264_1265del
ENST00000479320.5:n.1253+11_1253+12del
ENST00000495183.5:n.1255+11_1255+12del
ENST00000496081.5:n.840_841del
NM_002116.7:c.1012+11_1012+12del	NP_002107.3:n.1012+11_1012+12del
NM_002116.8:c.1012+11_1012+12del MANE Select	NP_002107.3:n.1012+11_1012+12del