Canonical Allele Identifier: CA2677794631
Gene: HLA-A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29943038_29943039insT , CM000668.2:g.29943038_29943039insT GRCh38
NC_000006.11:g.29910815_29910816insT , CM000668.1:g.29910815_29910816insT GRCh37
NC_000006.10:g.30018794_30018795insT NCBI36
NG_029217.2:g.5573_5574insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.343+12_343+13insT ENSP00000492789.2:n.343+12_343+13insT
ENST00000706892.1:n.619+12_619+13insT
ENST00000706893.1:c.343+12_343+13insT ENSP00000516609.1:n.343+12_343+13insT
ENST00000706894.1:c.343+12_343+13insT ENSP00000516610.1:n.343+12_343+13insT
ENST00000706895.1:n.619+12_619+13insT
ENST00000706896.1:n.619+12_619+13insT
ENST00000706897.1:n.619+12_619+13insT
ENST00000706898.1:c.343+12_343+13insT ENSP00000516611.1:n.343+12_343+13insT
ENST00000706899.1:n.619+12_619+13insT
ENST00000706900.1:c.259+12_259+13insT ENSP00000516617.1:n.259+12_259+13insT
ENST00000706901.1:c.343+12_343+13insT ENSP00000516612.1:n.343+12_343+13insT
ENST00000706902.1:c.343+12_343+13insT ENSP00000516613.1:n.343+12_343+13insT
ENST00000706903.1:c.343+12_343+13insT ENSP00000516614.1:n.343+12_343+13insT
ENST00000706904.1:c.343+12_343+13insT ENSP00000516615.1:n.343+12_343+13insT
ENST00000706905.1:c.343+12_343+13insT ENSP00000516616.1:n.343+12_343+13insT
ENST00000376809.10:c.343+12_343+13insT MANE Select ENSP00000366005.5:n.343+12_343+13insT
ENST00000638375.1:c.343+12_343+13insT ENSP00000492789.1:n.343+12_343+13insT
ENST00000376802.2:c.343+12_343+13insT ENSP00000365998.2:n.343+12_343+13insT
ENST00000376806.9:c.343+12_343+13insT ENSP00000366002.5:n.343+12_343+13insT
ENST00000376809.9:c.343+12_343+13insT ENSP00000366005.5:n.343+12_343+13insT
ENST00000396634.5:c.343+12_343+13insT ENSP00000379873.1:n.343+12_343+13insT
ENST00000429656.1:n.29_30insA
ENST00000461903.1:n.355_356insT
ENST00000479320.5:n.355_356insT
ENST00000495183.5:n.357_358insT
ENST00000496081.5:n.177+184_177+185insT
NM_002116.7:c.343+12_343+13insT NP_002107.3:n.343+12_343+13insT
NM_002116.8:c.343+12_343+13insT MANE Select NP_002107.3:n.343+12_343+13insT