Canonical Allele Identifier: CA1087467510
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356228_31356229insTT , CM000668.2:g.31356228_31356229insTT GRCh38
NC_000006.11:g.31324005_31324006insTT , CM000668.1:g.31324005_31324006insTT GRCh37
NC_000006.10:g.31431984_31431985insTT NCBI36
NG_023187.1:g.5984_5985insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.2030_2031insAA
ENST00000481849.6:n.2030_2031insAA
ENST00000497377.6:n.2030_2031insAA
ENST00000640094.2:c.557_558insAA ENSP00000491275.2:p.Glu187ThrfsTer28
ENST00000696558.1:c.557_558insAA ENSP00000512716.1:p.Glu187ThrfsTer?
ENST00000696559.1:c.557_558insAA ENSP00000512717.1:p.Glu187ThrfsTer28
ENST00000696560.1:c.557_558insAA ENSP00000512718.1:p.Glu187ThrfsTer28
ENST00000696561.1:c.557_558insAA ENSP00000512719.1:p.Glu187ThrfsTer28
ENST00000696562.1:c.557_558insAA ENSP00000512720.1:p.Glu187ThrfsTer28
ENST00000412585.7:c.557_558insAA MANE Select ENSP00000399168.2:p.Glu187ThrfsTer28
ENST00000412585.6:c.557_558insAA ENSP00000399168.2:p.Glu187ThrfsTer28
ENST00000434333.1:c.590_591insAA ENSP00000405931.1:p.Glu198ThrfsTer28
ENST00000474381.1:n.432_433insAA
ENST00000498007.1:n.823_824insAA
NM_005514.6:c.557_558insAA NP_005505.2:p.Glu187ThrfsTer28
XM_011514556.1:c.590_591insAA XP_011512858.1:p.Glu198ThrfsTer28
XM_011514557.1:c.557_558insAA XP_011512859.1:p.Glu187ThrfsTer28
XR_926175.1:n.567_568insAA
NM_005514.7:c.557_558insAA NP_005505.2:p.Glu187ThrfsTer28
NM_005514.8:c.557_558insAA MANE Select NP_005505.2:p.Glu187ThrfsTer28