Canonical Allele Identifier: CA136025143
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs45453496
MyVariant Identifiers: chr6:g.29912275del (hg19) chr6:g.29944498del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29944498del , CM000668.2:g.29944498del GRCh38
NC_000006.11:g.29912275del , CM000668.1:g.29912275del GRCh37
NC_000006.10:g.30020254del NCBI36
NG_029217.2:g.7034del

Transcript Alleles

HGVS Amino-acid change
ENST00000638375.2:c.895+101del ENSP00000492789.2:n.895+101del
ENST00000706892.1:n.1850del
ENST00000706893.1:c.928del ENSP00000516609.1:p.Arg310GlufsTer?
ENST00000706894.1:c.896-2del ENSP00000516610.1:n.896-2del
ENST00000706895.1:n.1272del
ENST00000706896.1:n.1750-2del
ENST00000706897.1:n.1172-2del
ENST00000706898.1:c.896-2del ENSP00000516611.1:n.896-2del
ENST00000706899.1:n.1750-2del
ENST00000706900.1:c.812-2del ENSP00000516617.1:n.812-2del
ENST00000706901.1:c.896-2del ENSP00000516612.1:n.896-2del
ENST00000706902.1:c.896-2del ENSP00000516613.1:n.896-2del
ENST00000706903.1:c.896-2del ENSP00000516614.1:n.896-2del
ENST00000706904.1:c.896-2del ENSP00000516615.1:n.896-2del
ENST00000706905.1:c.896-2del ENSP00000516616.1:n.896-2del
ENST00000376809.10:c.896-2del MANE Select ENSP00000366005.5:n.896-2del
ENST00000638375.1:c.895+101del ENSP00000492789.1:n.895+101del
ENST00000376802.2:c.895+101del ENSP00000365998.2:n.895+101del
ENST00000376806.9:c.896-2del ENSP00000366002.5:n.896-2del
ENST00000376809.9:c.896-2del ENSP00000366005.5:n.896-2del
ENST00000396634.5:c.896-2del ENSP00000379873.1:n.896-2del
ENST00000461903.1:n.1137-2del
ENST00000479320.5:n.1137-2del
ENST00000495183.5:n.1139-2del
ENST00000496081.5:n.713-2del
NM_002116.7:c.896-2del NP_002107.3:n.896-2del
NM_002116.8:c.896-2del MANE Select NP_002107.3:n.896-2del
Search 100 bp 5'
Search 100 bp 3'