Canonical Allele Identifier: CA2677957705
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356760_31356763del , CM000668.2:g.31356760_31356763del GRCh38
NC_000006.11:g.31324537_31324540del , CM000668.1:g.31324537_31324540del GRCh37
NC_000006.10:g.31432516_31432519del NCBI36
NG_023187.1:g.5451_5454del

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1742_1745del
ENST00000481849.6:n.1742_1745del
ENST00000497377.6:n.1742_1745del
ENST00000640094.2:c.269_272del ENSP00000491275.2:p.Ile90ThrfsTer?
ENST00000696558.1:c.269_272del ENSP00000512716.1:p.Ile90ThrfsTer?
ENST00000696559.1:c.269_272del ENSP00000512717.1:p.Ile90ThrfsTer?
ENST00000696560.1:c.269_272del ENSP00000512718.1:p.Ile90ThrfsTer?
ENST00000696561.1:c.269_272del ENSP00000512719.1:p.Ile90ThrfsTer?
ENST00000696562.1:c.269_272del ENSP00000512720.1:p.Ile90ThrfsTer?
ENST00000412585.7:c.269_272del MANE Select ENSP00000399168.2:p.Ile90ThrfsTer?
ENST00000412585.6:c.269_272del ENSP00000399168.2:p.Ile90ThrfsTer?
ENST00000434333.1:c.302_305del ENSP00000405931.1:p.Ile101ThrfsTer?
ENST00000474381.1:n.144_147del
ENST00000498007.1:n.290_293del
ENST00000603274.1:n.114_117del
NM_005514.6:c.269_272del NP_005505.2:p.Ile90ThrfsTer?
XM_011514556.1:c.302_305del XP_011512858.1:p.Ile101ThrfsTer?
XM_011514557.1:c.269_272del XP_011512859.1:p.Ile90ThrfsTer?
XR_926175.1:n.279_282del
NM_005514.7:c.269_272del NP_005505.2:p.Ile90ThrfsTer?
NM_005514.8:c.269_272del MANE Select NP_005505.2:p.Ile90ThrfsTer?