Canonical Allele Identifier: CA2770464000
Gene: HLA-A HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29945326_29945327insTTCT , CM000668.2:g.29945326_29945327insTTCT GRCh38
NC_000006.11:g.29913103_29913104insTTCT , CM000668.1:g.29913103_29913104insTTCT GRCh37
NC_000006.10:g.30021082_30021083insTTCT NCBI36
NG_029217.2:g.7862_7863insTTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.976+45_976+46insTTCT ENSP00000492789.2:n.976+45_976+46insTTCT
ENST00000706892.1:n.2678_2679insTTCT
ENST00000706893.1:c.*77+45_*77+46insTTCT ENSP00000516609.1:n.*77+45_*77+46insTTCT
ENST00000706894.1:c.1138_1139insTTCT ENSP00000516610.1:p.Gln380LeufsTer24
ENST00000706895.1:n.1958_1959insTTCT
ENST00000706896.1:n.2389+45_2389+46insTTCT
ENST00000706897.1:n.1811+45_1811+46insTTCT
ENST00000706898.1:c.1111+45_1111+46insTTCT ENSP00000516611.1:n.1111+45_1111+46insTTCT
ENST00000706899.1:n.1947+45_1947+46insTTCT
ENST00000706900.1:c.1009+45_1009+46insTTCT ENSP00000516617.1:n.1009+45_1009+46insTTCT
ENST00000706901.1:c.1093+45_1093+46insTTCT ENSP00000516612.1:n.1093+45_1093+46insTTCT
ENST00000706902.1:c.1093+45_1093+46insTTCT ENSP00000516613.1:n.1093+45_1093+46insTTCT
ENST00000706903.1:c.1093+45_1093+46insTTCT ENSP00000516614.1:n.1093+45_1093+46insTTCT
ENST00000706904.1:c.1093+45_1093+46insTTCT ENSP00000516615.1:n.1093+45_1093+46insTTCT
ENST00000706905.1:c.1093+45_1093+46insTTCT ENSP00000516616.1:n.1093+45_1093+46insTTCT
ENST00000376809.10:c.1093+45_1093+46insTTCT MANE Select ENSP00000366005.5:n.1093+45_1093+46insTTCT
ENST00000376802.2:c.896-125_896-124insTTCT ENSP00000365998.2:n.896-125_896-124insTTCT
ENST00000376806.9:c.1111+45_1111+46insTTCT ENSP00000366002.5:n.1111+45_1111+46insTTCT
ENST00000376809.9:c.1093+45_1093+46insTTCT ENSP00000366005.5:n.1093+45_1093+46insTTCT
ENST00000396634.5:c.1093+45_1093+46insTTCT ENSP00000379873.1:n.1093+45_1093+46insTTCT
ENST00000495183.5:n.1332+45_1332+46insTTCT
ENST00000496081.5:n.1352+45_1352+46insTTCT
NM_002116.7:c.1093+45_1093+46insTTCT NP_002107.3:n.1093+45_1093+46insTTCT
NM_002116.8:c.1093+45_1093+46insTTCT MANE Select NP_002107.3:n.1093+45_1093+46insTTCT
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