Canonical Allele Identifier: CA1814482937

Gene: TNFRSF11B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118947955_118947956delinsCT , CM000670.2:g.118947955_118947956delinsCT	GRCh38
NC_000008.10:g.119960194_119960195delinsCT , CM000670.1:g.119960194_119960195delinsCT	GRCh37
NC_000008.9:g.120029375_120029376delinsCT	NCBI36
NG_012202.1:g.9189_9190delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297350.9:c.30+3836_30+3837delinsAG MANE Select	ENSP00000297350.4:n.30+3836_30+3837delinsAG
ENST00000297350.8:c.30+3836_30+3837delinsAG	ENSP00000297350.4:n.30+3836_30+3837delinsAG
ENST00000517352.1:c.30+3836_30+3837delinsAG	ENSP00000427924.1:n.30+3836_30+3837delinsAG
NM_002546.3:c.30+3836_30+3837delinsAG	NP_002537.3:n.30+3836_30+3837delinsAG
NM_002546.4:c.30+3836_30+3837delinsAG MANE Select	NP_002537.3:n.30+3836_30+3837delinsAG