Canonical Allele Identifier: CA2677957625
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356713_31356714insAGCAGGGTC , CM000668.2:g.31356713_31356714insAGCAGGGTC GRCh38
NC_000006.11:g.31324490_31324491insAGCAGGGTC , CM000668.1:g.31324490_31324491insAGCAGGGTC GRCh37
NC_000006.10:g.31432469_31432470insAGCAGGGTC NCBI36
NG_023187.1:g.5499_5500insGACCCTGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1790_1791insGACCCTGCT
ENST00000481849.6:n.1790_1791insGACCCTGCT
ENST00000497377.6:n.1790_1791insGACCCTGCT
ENST00000640094.2:c.317_318insGACCCTGCT ENSP00000491275.2:p.Arg106_Gly107insThrLeuLeu
ENST00000696558.1:c.317_318insGACCCTGCT ENSP00000512716.1:p.Arg106_Gly107insThrLeuLeu
ENST00000696559.1:c.317_318insGACCCTGCT ENSP00000512717.1:p.Arg106_Gly107insThrLeuLeu
ENST00000696560.1:c.317_318insGACCCTGCT ENSP00000512718.1:p.Arg106_Gly107insThrLeuLeu
ENST00000696561.1:c.317_318insGACCCTGCT ENSP00000512719.1:p.Arg106_Gly107insThrLeuLeu
ENST00000696562.1:c.317_318insGACCCTGCT ENSP00000512720.1:p.Arg106_Gly107insThrLeuLeu
ENST00000412585.7:c.317_318insGACCCTGCT MANE Select ENSP00000399168.2:p.Arg106_Gly107insThrLeuLeu
ENST00000412585.6:c.317_318insGACCCTGCT ENSP00000399168.2:p.Arg106_Gly107insThrLeuLeu
ENST00000434333.1:c.350_351insGACCCTGCT ENSP00000405931.1:p.Arg117_Gly118insThrLeuLeu
ENST00000474381.1:n.192_193insGACCCTGCT
ENST00000498007.1:n.338_339insGACCCTGCT
ENST00000603274.1:n.67_68insAGCAGGGTC
NM_005514.6:c.317_318insGACCCTGCT NP_005505.2:p.Arg106_Gly107insThrLeuLeu
XM_011514556.1:c.350_351insGACCCTGCT XP_011512858.1:p.Arg117_Gly118insThrLeuLeu
XM_011514557.1:c.317_318insGACCCTGCT XP_011512859.1:p.Arg106_Gly107insThrLeuLeu
XR_926175.1:n.327_328insGACCCTGCT
NM_005514.7:c.317_318insGACCCTGCT NP_005505.2:p.Arg106_Gly107insThrLeuLeu
NM_005514.8:c.317_318insGACCCTGCT MANE Select NP_005505.2:p.Arg106_Gly107insThrLeuLeu