Canonical Allele Identifier: CA2843661994
Gene: HLA-A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29943278_29943279insT , CM000668.2:g.29943278_29943279insT GRCh38
NC_000006.11:g.29911055_29911056insT , CM000668.1:g.29911055_29911056insT GRCh37
NC_000006.10:g.30019034_30019035insT NCBI36
NG_029217.2:g.5813_5814insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.354_355insT ENSP00000492789.2:p.Ile119TyrfsTer?
ENST00000706892.1:n.630_631insT
ENST00000706893.1:c.354_355insT ENSP00000516609.1:p.Ile119TyrfsTer?
ENST00000706894.1:c.354_355insT ENSP00000516610.1:p.Ile119TyrfsTer?
ENST00000706895.1:n.630_631insT
ENST00000706896.1:n.630_631insT
ENST00000706897.1:n.630_631insT
ENST00000706898.1:c.354_355insT ENSP00000516611.1:p.Ile119TyrfsTer?
ENST00000706899.1:n.630_631insT
ENST00000706900.1:c.270_271insT ENSP00000516617.1:p.Ile91TyrfsTer?
ENST00000706901.1:c.354_355insT ENSP00000516612.1:p.Ile119TyrfsTer?
ENST00000706902.1:c.354_355insT ENSP00000516613.1:p.Ile119TyrfsTer?
ENST00000706903.1:c.354_355insT ENSP00000516614.1:p.Ile119TyrfsTer?
ENST00000706904.1:c.354_355insT ENSP00000516615.1:p.Ile119TyrfsTer?
ENST00000706905.1:c.354_355insT ENSP00000516616.1:p.Ile119TyrfsTer?
ENST00000376809.10:c.354_355insT MANE Select ENSP00000366005.5:p.Ile119TyrfsTer?
ENST00000638375.1:c.354_355insT ENSP00000492789.1:p.Ile119TyrfsTer?
ENST00000376802.2:c.354_355insT ENSP00000365998.2:p.Ile119TyrfsTer?
ENST00000376806.9:c.354_355insT ENSP00000366002.5:p.Ile119TyrfsTer?
ENST00000376809.9:c.354_355insT ENSP00000366005.5:p.Ile119TyrfsTer?
ENST00000396634.5:c.354_355insT ENSP00000379873.1:p.Ile119TyrfsTer?
ENST00000461903.1:n.595_596insT
ENST00000479320.5:n.595_596insT
ENST00000495183.5:n.597_598insT
ENST00000496081.5:n.178-7_178-6insT
NM_002116.7:c.354_355insT NP_002107.3:p.Ile119TyrfsTer?
NM_002116.8:c.354_355insT MANE Select NP_002107.3:p.Ile119TyrfsTer?