Canonical Allele Identifier: CA1814477166
Gene: TNFRSF11B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118939498_118939500delinsTGA , CM000670.2:g.118939498_118939500delinsTGA GRCh38
NC_000008.10:g.119951737_119951739delinsTGA , CM000670.1:g.119951737_119951739delinsTGA GRCh37
NC_000008.9:g.120020918_120020920delinsTGA NCBI36
NG_012202.1:g.17645_17647delinsTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.31-6200_31-6198delinsTCA MANE Select ENSP00000297350.4:n.31-6200_31-6198delinsTCA
ENST00000297350.8:c.31-6200_31-6198delinsTCA ENSP00000297350.4:n.31-6200_31-6198delinsTCA
ENST00000517352.1:c.31-6200_31-6198delinsTCA ENSP00000427924.1:n.31-6200_31-6198delinsTCA
NM_002546.3:c.31-6200_31-6198delinsTCA NP_002537.3:n.31-6200_31-6198delinsTCA
NM_002546.4:c.31-6200_31-6198delinsTCA MANE Select NP_002537.3:n.31-6200_31-6198delinsTCA
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