Canonical Allele Identifier: CA1087469572
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356760_31356764del , CM000668.2:g.31356760_31356764del GRCh38
NC_000006.11:g.31324537_31324541del , CM000668.1:g.31324537_31324541del GRCh37
NC_000006.10:g.31432516_31432520del NCBI36
NG_023187.1:g.5449_5453del

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1740_1744del
ENST00000481849.6:n.1740_1744del
ENST00000497377.6:n.1740_1744del
ENST00000640094.2:c.267_271del ENSP00000491275.2:p.Ile90GlnfsTer7
ENST00000696558.1:c.267_271del ENSP00000512716.1:p.Ile90GlnfsTer7
ENST00000696559.1:c.267_271del ENSP00000512717.1:p.Ile90GlnfsTer7
ENST00000696560.1:c.267_271del ENSP00000512718.1:p.Ile90GlnfsTer7
ENST00000696561.1:c.267_271del ENSP00000512719.1:p.Ile90GlnfsTer7
ENST00000696562.1:c.267_271del ENSP00000512720.1:p.Ile90GlnfsTer7
ENST00000412585.7:c.267_271del MANE Select ENSP00000399168.2:p.Ile90GlnfsTer7
ENST00000412585.6:c.267_271del ENSP00000399168.2:p.Ile90GlnfsTer7
ENST00000434333.1:c.300_304del ENSP00000405931.1:p.Ile101GlnfsTer7
ENST00000474381.1:n.142_146del
ENST00000498007.1:n.288_292del
ENST00000603274.1:n.114_118del
NM_005514.6:c.267_271del NP_005505.2:p.Ile90GlnfsTer7
XM_011514556.1:c.300_304del XP_011512858.1:p.Ile101GlnfsTer7
XM_011514557.1:c.267_271del XP_011512859.1:p.Ile90GlnfsTer7
XR_926175.1:n.277_281del
NM_005514.7:c.267_271del NP_005505.2:p.Ile90GlnfsTer7
NM_005514.8:c.267_271del MANE Select NP_005505.2:p.Ile90GlnfsTer7