Canonical Allele Identifier: CA1087469608
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356763_31356764insTTCC , CM000668.2:g.31356763_31356764insTTCC GRCh38
NC_000006.11:g.31324540_31324541insTTCC , CM000668.1:g.31324540_31324541insTTCC GRCh37
NC_000006.10:g.31432519_31432520insTTCC NCBI36
NG_023187.1:g.5449_5450insGGAA

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1740_1741insGGAA
ENST00000481849.6:n.1740_1741insGGAA
ENST00000497377.6:n.1740_1741insGGAA
ENST00000640094.2:c.267_268insGGAA ENSP00000491275.2:p.Ile90GlyfsTer10
ENST00000696558.1:c.267_268insGGAA ENSP00000512716.1:p.Ile90GlyfsTer10
ENST00000696559.1:c.267_268insGGAA ENSP00000512717.1:p.Ile90GlyfsTer10
ENST00000696560.1:c.267_268insGGAA ENSP00000512718.1:p.Ile90GlyfsTer10
ENST00000696561.1:c.267_268insGGAA ENSP00000512719.1:p.Ile90GlyfsTer10
ENST00000696562.1:c.267_268insGGAA ENSP00000512720.1:p.Ile90GlyfsTer10
ENST00000412585.7:c.267_268insGGAA MANE Select ENSP00000399168.2:p.Ile90GlyfsTer10
ENST00000412585.6:c.267_268insGGAA ENSP00000399168.2:p.Ile90GlyfsTer10
ENST00000434333.1:c.300_301insGGAA ENSP00000405931.1:p.Ile101GlyfsTer10
ENST00000474381.1:n.142_143insGGAA
ENST00000498007.1:n.288_289insGGAA
ENST00000603274.1:n.117_118insTTCC
NM_005514.6:c.267_268insGGAA NP_005505.2:p.Ile90GlyfsTer10
XM_011514556.1:c.300_301insGGAA XP_011512858.1:p.Ile101GlyfsTer10
XM_011514557.1:c.267_268insGGAA XP_011512859.1:p.Ile90GlyfsTer10
XR_926175.1:n.277_278insGGAA
NM_005514.7:c.267_268insGGAA NP_005505.2:p.Ile90GlyfsTer10
NM_005514.8:c.267_268insGGAA MANE Select NP_005505.2:p.Ile90GlyfsTer10