Canonical Allele Identifier: CA2677794902
Gene: HLA-A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29943117_29943118insT , CM000668.2:g.29943117_29943118insT GRCh38
NC_000006.11:g.29910894_29910895insT , CM000668.1:g.29910894_29910895insT GRCh37
NC_000006.10:g.30018873_30018874insT NCBI36
NG_029217.2:g.5652_5653insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.343+91_343+92insT ENSP00000492789.2:n.343+91_343+92insT
ENST00000706892.1:n.619+91_619+92insT
ENST00000706893.1:c.343+91_343+92insT ENSP00000516609.1:n.343+91_343+92insT
ENST00000706894.1:c.343+91_343+92insT ENSP00000516610.1:n.343+91_343+92insT
ENST00000706895.1:n.619+91_619+92insT
ENST00000706896.1:n.619+91_619+92insT
ENST00000706897.1:n.619+91_619+92insT
ENST00000706898.1:c.343+91_343+92insT ENSP00000516611.1:n.343+91_343+92insT
ENST00000706899.1:n.619+91_619+92insT
ENST00000706900.1:c.259+91_259+92insT ENSP00000516617.1:n.259+91_259+92insT
ENST00000706901.1:c.343+91_343+92insT ENSP00000516612.1:n.343+91_343+92insT
ENST00000706902.1:c.343+91_343+92insT ENSP00000516613.1:n.343+91_343+92insT
ENST00000706903.1:c.343+91_343+92insT ENSP00000516614.1:n.343+91_343+92insT
ENST00000706904.1:c.343+91_343+92insT ENSP00000516615.1:n.343+91_343+92insT
ENST00000706905.1:c.343+91_343+92insT ENSP00000516616.1:n.343+91_343+92insT
ENST00000376809.10:c.343+91_343+92insT MANE Select ENSP00000366005.5:n.343+91_343+92insT
ENST00000638375.1:c.343+91_343+92insT ENSP00000492789.1:n.343+91_343+92insT
ENST00000376802.2:c.343+91_343+92insT ENSP00000365998.2:n.343+91_343+92insT
ENST00000376806.9:c.343+91_343+92insT ENSP00000366002.5:n.343+91_343+92insT
ENST00000376809.9:c.343+91_343+92insT ENSP00000366005.5:n.343+91_343+92insT
ENST00000396634.5:c.343+91_343+92insT ENSP00000379873.1:n.343+91_343+92insT
ENST00000461903.1:n.434_435insT
ENST00000479320.5:n.434_435insT
ENST00000495183.5:n.436_437insT
ENST00000496081.5:n.178-168_178-167insT
NM_002116.7:c.343+91_343+92insT NP_002107.3:n.343+91_343+92insT
NM_002116.8:c.343+91_343+92insT MANE Select NP_002107.3:n.343+91_343+92insT