Canonical Allele Identifier: CA1814482932
Gene: TNFRSF11B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118947947_118947951delinsATTAC , CM000670.2:g.118947947_118947951delinsATTAC GRCh38
NC_000008.10:g.119960186_119960190delinsATTAC , CM000670.1:g.119960186_119960190delinsATTAC GRCh37
NC_000008.9:g.120029367_120029371delinsATTAC NCBI36
NG_012202.1:g.9194_9198delinsGTAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.30+3841_30+3845delinsGTAAT MANE Select ENSP00000297350.4:n.30+3841_30+3845delinsGTAAT
ENST00000297350.8:c.30+3841_30+3845delinsGTAAT ENSP00000297350.4:n.30+3841_30+3845delinsGTAAT
ENST00000517352.1:c.30+3841_30+3845delinsGTAAT ENSP00000427924.1:n.30+3841_30+3845delinsGTAAT
NM_002546.3:c.30+3841_30+3845delinsGTAAT NP_002537.3:n.30+3841_30+3845delinsGTAAT
NM_002546.4:c.30+3841_30+3845delinsGTAAT MANE Select NP_002537.3:n.30+3841_30+3845delinsGTAAT
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