Canonical Allele Identifier: CA650785885
Gene: HLA-B HGNC NCBI

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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31354138_31354139insG , CM000668.2:g.31354138_31354139insG GRCh38
NC_000006.11:g.31321915_31321916insG , CM000668.1:g.31321915_31321916insG GRCh37
NC_000006.10:g.31429894_31429895insG NCBI36
NG_023187.1:g.8074_8075insC

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.3298_3299insC
ENST00000481849.6:n.3258_3259insC
ENST00000497377.6:n.3165_3166insC
ENST00000696558.1:c.1320_1321insC ENSP00000512716.1:n.1320_1321insC
ENST00000696559.1:c.*162_*163insC ENSP00000512717.1:n.*162_*163insC
ENST00000696560.1:c.*162_*163insC ENSP00000512718.1:n.*162_*163insC
ENST00000696561.1:c.*162_*163insC ENSP00000512719.1:n.*162_*163insC
ENST00000696562.1:c.*162_*163insC ENSP00000512720.1:n.*162_*163insC
ENST00000412585.7:c.*162_*163insC MANE Select ENSP00000399168.2:n.*162_*163insC
ENST00000412585.6:c.*162_*163insC ENSP00000399168.2:n.*162_*163insC
ENST00000481849.5:n.486_487insC
ENST00000497377.5:n.650_651insC
NM_005514.6:c.*162_*163insC NP_005505.2:n.*162_*163insC
XM_011514556.1:c.*162_*163insC XP_011512858.1:n.*162_*163insC
XM_011514557.1:c.*162_*163insC XP_011512859.1:n.*162_*163insC
XR_926175.1:n.1690_1691insC
NM_005514.7:c.*162_*163insC NP_005505.2:n.*162_*163insC
NM_005514.8:c.*162_*163insC MANE Select NP_005505.2:n.*162_*163insC
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