Canonical Allele Identifier: CA2677957656
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356731_31356732insA , CM000668.2:g.31356731_31356732insA GRCh38
NC_000006.11:g.31324508_31324509insA , CM000668.1:g.31324508_31324509insA GRCh37
NC_000006.10:g.31432487_31432488insA NCBI36
NG_023187.1:g.5481_5482insT

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1772_1773insT
ENST00000481849.6:n.1772_1773insT
ENST00000497377.6:n.1772_1773insT
ENST00000640094.2:c.299_300insT ENSP00000491275.2:p.Glu100AspfsTer?
ENST00000696558.1:c.299_300insT ENSP00000512716.1:p.Glu100AspfsTer?
ENST00000696559.1:c.299_300insT ENSP00000512717.1:p.Glu100AspfsTer?
ENST00000696560.1:c.299_300insT ENSP00000512718.1:p.Glu100AspfsTer?
ENST00000696561.1:c.299_300insT ENSP00000512719.1:p.Glu100AspfsTer?
ENST00000696562.1:c.299_300insT ENSP00000512720.1:p.Glu100AspfsTer?
ENST00000412585.7:c.299_300insT MANE Select ENSP00000399168.2:p.Glu100AspfsTer?
ENST00000412585.6:c.299_300insT ENSP00000399168.2:p.Glu100AspfsTer?
ENST00000434333.1:c.332_333insT ENSP00000405931.1:p.Glu111AspfsTer?
ENST00000474381.1:n.174_175insT
ENST00000498007.1:n.320_321insT
ENST00000603274.1:n.85_86insA
NM_005514.6:c.299_300insT NP_005505.2:p.Glu100AspfsTer?
XM_011514556.1:c.332_333insT XP_011512858.1:p.Glu111AspfsTer?
XM_011514557.1:c.299_300insT XP_011512859.1:p.Glu100AspfsTer?
XR_926175.1:n.309_310insT
NM_005514.7:c.299_300insT NP_005505.2:p.Glu100AspfsTer?
NM_005514.8:c.299_300insT MANE Select NP_005505.2:p.Glu100AspfsTer?