Canonical Allele Identifier: CA1087467508
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356227_31356228insAG , CM000668.2:g.31356227_31356228insAG GRCh38
NC_000006.11:g.31324004_31324005insAG , CM000668.1:g.31324004_31324005insAG GRCh37
NC_000006.10:g.31431983_31431984insAG NCBI36
NG_023187.1:g.5985_5986insCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.2031_2032insCT
ENST00000481849.6:n.2031_2032insCT
ENST00000497377.6:n.2031_2032insCT
ENST00000640094.2:c.558_559insCT ENSP00000491275.2:p.Glu187LeufsTer28
ENST00000696558.1:c.558_559insCT ENSP00000512716.1:p.Glu187LeufsTer?
ENST00000696559.1:c.558_559insCT ENSP00000512717.1:p.Glu187LeufsTer28
ENST00000696560.1:c.558_559insCT ENSP00000512718.1:p.Glu187LeufsTer28
ENST00000696561.1:c.558_559insCT ENSP00000512719.1:p.Glu187LeufsTer28
ENST00000696562.1:c.558_559insCT ENSP00000512720.1:p.Glu187LeufsTer28
ENST00000412585.7:c.558_559insCT MANE Select ENSP00000399168.2:p.Glu187LeufsTer28
ENST00000412585.6:c.558_559insCT ENSP00000399168.2:p.Glu187LeufsTer28
ENST00000434333.1:c.591_592insCT ENSP00000405931.1:p.Glu198LeufsTer28
ENST00000474381.1:n.433_434insCT
ENST00000498007.1:n.824_825insCT
NM_005514.6:c.558_559insCT NP_005505.2:p.Glu187LeufsTer28
XM_011514556.1:c.591_592insCT XP_011512858.1:p.Glu198LeufsTer28
XM_011514557.1:c.558_559insCT XP_011512859.1:p.Glu187LeufsTer28
XR_926175.1:n.568_569insCT
NM_005514.7:c.558_559insCT NP_005505.2:p.Glu187LeufsTer28
NM_005514.8:c.558_559insCT MANE Select NP_005505.2:p.Glu187LeufsTer28