Canonical Allele Identifier: CA2677795864
Gene: HLA-A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29943291_29943294del , CM000668.2:g.29943291_29943294del GRCh38
NC_000006.11:g.29911068_29911071del , CM000668.1:g.29911068_29911071del GRCh37
NC_000006.10:g.30019047_30019050del NCBI36
NG_029217.2:g.5826_5829del

Transcript Alleles

HGVS Amino-acid change
ENST00000638375.2:c.367_370del ENSP00000492789.2:p.Tyr123AlafsTer27
ENST00000706892.1:n.643_646del
ENST00000706893.1:c.367_370del ENSP00000516609.1:p.Tyr123AlafsTer27
ENST00000706894.1:c.367_370del ENSP00000516610.1:p.Tyr123AlafsTer27
ENST00000706895.1:n.643_646del
ENST00000706896.1:n.643_646del
ENST00000706897.1:n.643_646del
ENST00000706898.1:c.367_370del ENSP00000516611.1:p.Tyr123AlafsTer27
ENST00000706899.1:n.643_646del
ENST00000706900.1:c.283_286del ENSP00000516617.1:p.Tyr95AlafsTer27
ENST00000706901.1:c.367_370del ENSP00000516612.1:p.Tyr123AlafsTer27
ENST00000706902.1:c.367_370del ENSP00000516613.1:p.Tyr123AlafsTer27
ENST00000706903.1:c.367_370del ENSP00000516614.1:p.Tyr123AlafsTer27
ENST00000706904.1:c.367_370del ENSP00000516615.1:p.Tyr123AlafsTer27
ENST00000706905.1:c.367_370del ENSP00000516616.1:p.Tyr123AlafsTer27
ENST00000376809.10:c.367_370del MANE Select ENSP00000366005.5:p.Tyr123AlafsTer27
ENST00000638375.1:c.367_370del ENSP00000492789.1:p.Tyr123AlafsTer27
ENST00000376802.2:c.367_370del ENSP00000365998.2:p.Tyr123AlafsTer27
ENST00000376806.9:c.367_370del ENSP00000366002.5:p.Tyr123AlafsTer27
ENST00000376809.9:c.367_370del ENSP00000366005.5:p.Tyr123AlafsTer27
ENST00000396634.5:c.367_370del ENSP00000379873.1:p.Tyr123AlafsTer27
ENST00000461903.1:n.608_611del
ENST00000479320.5:n.608_611del
ENST00000495183.5:n.610_613del
ENST00000496081.5:n.184_187del
NM_002116.7:c.367_370del NP_002107.3:p.Tyr123AlafsTer27
NM_002116.8:c.367_370del MANE Select NP_002107.3:p.Tyr123AlafsTer27