Canonical Allele Identifier: CA2677796571
Gene: HLA-A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29945260_29945261insC , CM000668.2:g.29945260_29945261insC GRCh38
NC_000006.11:g.29913037_29913038insC , CM000668.1:g.29913037_29913038insC GRCh37
NC_000006.10:g.30021016_30021017insC NCBI36
NG_029217.2:g.7796_7797insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.955_956insC ENSP00000492789.2:p.Val319AlafsTer7
ENST00000706892.1:n.2612_2613insC
ENST00000706893.1:c.*56_*57insC ENSP00000516609.1:n.*56_*57insC
ENST00000706894.1:c.1072_1073insC ENSP00000516610.1:p.Val358AlafsTer7
ENST00000706895.1:n.1892_1893insC
ENST00000706896.1:n.2368_2369insC
ENST00000706897.1:n.1790_1791insC
ENST00000706898.1:c.1090_1091insC ENSP00000516611.1:p.Val364AlafsTer7
ENST00000706899.1:n.1926_1927insC
ENST00000706900.1:c.988_989insC ENSP00000516617.1:p.Val330AlafsTer7
ENST00000706901.1:c.1072_1073insC ENSP00000516612.1:p.Val358AlafsTer7
ENST00000706902.1:c.1072_1073insC ENSP00000516613.1:p.Val358AlafsTer7
ENST00000706903.1:c.1072_1073insC ENSP00000516614.1:p.Val358AlafsTer7
ENST00000706904.1:c.1072_1073insC ENSP00000516615.1:p.Val358AlafsTer7
ENST00000706905.1:c.1072_1073insC ENSP00000516616.1:p.Val358AlafsTer7
ENST00000376809.10:c.1072_1073insC MANE Select ENSP00000366005.5:p.Val358AlafsTer7
ENST00000638375.1:c.955_956insC ENSP00000492789.1:p.Val319AlafsTer7
ENST00000376802.2:c.896-191_896-190insC ENSP00000365998.2:n.896-191_896-190insC
ENST00000376806.9:c.1090_1091insC ENSP00000366002.5:p.Val364AlafsTer7
ENST00000376809.9:c.1072_1073insC ENSP00000366005.5:p.Val358AlafsTer7
ENST00000396634.5:c.1072_1073insC ENSP00000379873.1:p.Val358AlafsTer7
ENST00000461903.1:n.1331_1332insC
ENST00000479320.5:n.1313_1314insC
ENST00000495183.5:n.1311_1312insC
ENST00000496081.5:n.1331_1332insC
NM_002116.7:c.1072_1073insC NP_002107.3:p.Val358AlafsTer7
NM_002116.8:c.1072_1073insC MANE Select NP_002107.3:p.Val358AlafsTer7