Canonical Allele Identifier: CA2677794727
Gene: HLA-A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29944551_29944552insG , CM000668.2:g.29944551_29944552insG GRCh38
NC_000006.11:g.29912328_29912329insG , CM000668.1:g.29912328_29912329insG GRCh37
NC_000006.10:g.30020307_30020308insG NCBI36
NG_029217.2:g.7087_7088insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.895+154_895+155insG ENSP00000492789.2:n.895+154_895+155insG
ENST00000706892.1:n.1903_1904insG
ENST00000706893.1:c.981_982insG ENSP00000516609.1:p.Ser328ValfsTer6
ENST00000706894.1:c.947_948insG ENSP00000516610.1:p.Leu317SerfsTer23
ENST00000706895.1:n.1325_1326insG
ENST00000706896.1:n.1801_1802insG
ENST00000706897.1:n.1223_1224insG
ENST00000706898.1:c.947_948insG ENSP00000516611.1:p.Leu317SerfsTer29
ENST00000706899.1:n.1801_1802insG
ENST00000706900.1:c.863_864insG ENSP00000516617.1:p.Leu289SerfsTer23
ENST00000706901.1:c.947_948insG ENSP00000516612.1:p.Leu317SerfsTer23
ENST00000706902.1:c.947_948insG ENSP00000516613.1:p.Leu317SerfsTer23
ENST00000706903.1:c.947_948insG ENSP00000516614.1:p.Leu317SerfsTer23
ENST00000706904.1:c.947_948insG ENSP00000516615.1:p.Leu317SerfsTer23
ENST00000706905.1:c.947_948insG ENSP00000516616.1:p.Leu317SerfsTer23
ENST00000376809.10:c.947_948insG MANE Select ENSP00000366005.5:p.Leu317SerfsTer23
ENST00000638375.1:c.895+154_895+155insG ENSP00000492789.1:n.895+154_895+155insG
ENST00000376802.2:c.895+154_895+155insG ENSP00000365998.2:n.895+154_895+155insG
ENST00000376806.9:c.947_948insG ENSP00000366002.5:p.Leu317SerfsTer29
ENST00000376809.9:c.947_948insG ENSP00000366005.5:p.Leu317SerfsTer23
ENST00000396634.5:c.947_948insG ENSP00000379873.1:p.Leu317SerfsTer23
ENST00000461903.1:n.1188_1189insG
ENST00000479320.5:n.1188_1189insG
ENST00000495183.5:n.1190_1191insG
ENST00000496081.5:n.764_765insG
NM_002116.7:c.947_948insG NP_002107.3:p.Leu317SerfsTer23
NM_002116.8:c.947_948insG MANE Select NP_002107.3:p.Leu317SerfsTer23