Canonical Allele Identifier: CA1814482915

Gene: TNFRSF11B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118947904_118947905delinsCA , CM000670.2:g.118947904_118947905delinsCA	GRCh38
NC_000008.10:g.119960143_119960144delinsCA , CM000670.1:g.119960143_119960144delinsCA	GRCh37
NC_000008.9:g.120029324_120029325delinsCA	NCBI36
NG_012202.1:g.9240_9241delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297350.9:c.30+3887_30+3888delinsTG MANE Select	ENSP00000297350.4:n.30+3887_30+3888delinsTG
ENST00000297350.8:c.30+3887_30+3888delinsTG	ENSP00000297350.4:n.30+3887_30+3888delinsTG
ENST00000517352.1:c.30+3887_30+3888delinsTG	ENSP00000427924.1:n.30+3887_30+3888delinsTG
NM_002546.3:c.30+3887_30+3888delinsTG	NP_002537.3:n.30+3887_30+3888delinsTG
NM_002546.4:c.30+3887_30+3888delinsTG MANE Select	NP_002537.3:n.30+3887_30+3888delinsTG