Canonical Allele Identifier: CA1087464669
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355159_31355160insGCCAGG , CM000668.2:g.31355159_31355160insGCCAGG GRCh38
NC_000006.11:g.31322936_31322937insGCCAGG , CM000668.1:g.31322936_31322937insGCCAGG GRCh37
NC_000006.10:g.31430915_31430916insGCCAGG NCBI36
NG_023187.1:g.7053_7054insCCTGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.3006_3007insCCTGGC
ENST00000481849.6:n.2525_2526insCCTGGC
ENST00000497377.6:n.2432_2433insCCTGGC
ENST00000640094.2:c.895+157_895+158insCCTGGC ENSP00000491275.2:n.895+157_895+158insCCTGGC
ENST00000696558.1:c.1028_1029insCCTGGC ENSP00000512716.1:n.1028_1029insCCTGGC
ENST00000696559.1:c.959_960insCCTGGC ENSP00000512717.1:p.Val320_Val321insLeuAla
ENST00000696560.1:c.959_960insCCTGGC ENSP00000512718.1:p.Val320_Val321insLeuAla
ENST00000696561.1:c.959_960insCCTGGC ENSP00000512719.1:p.Val320_Val321insLeuAla
ENST00000696562.1:c.959_960insCCTGGC ENSP00000512720.1:p.Val320_Val321insLeuAla
ENST00000412585.7:c.959_960insCCTGGC MANE Select ENSP00000399168.2:p.Val320_Val321insLeuAla
ENST00000640094.1:c.88+157_88+158insCCTGGC ENSP00000491275.1:n.88+157_88+158insCCTGGC
ENST00000412585.6:c.959_960insCCTGGC ENSP00000399168.2:p.Val320_Val321insLeuAla
ENST00000463574.1:n.550_551insCCTGGC
NM_005514.6:c.959_960insCCTGGC NP_005505.2:p.Val320_Val321insLeuAla
XM_011514556.1:c.992_993insCCTGGC XP_011512858.1:p.Val331_Val332insLeuAla
XM_011514557.1:c.895+157_895+158insCCTGGC XP_011512859.1:n.895+157_895+158insCCTGGC
XR_926175.1:n.1398_1399insCCTGGC
NM_005514.7:c.959_960insCCTGGC NP_005505.2:p.Val320_Val321insLeuAla
NM_005514.8:c.959_960insCCTGGC MANE Select NP_005505.2:p.Val320_Val321insLeuAla