Canonical Allele Identifier: CA1814470822

Gene: TNFRSF11B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118932860_118932861delinsGT , CM000670.2:g.118932860_118932861delinsGT	GRCh38
NC_000008.10:g.119945099_119945100delinsGT , CM000670.1:g.119945099_119945100delinsGT	GRCh37
NC_000008.9:g.120014280_120014281delinsGT	NCBI36
NG_012202.1:g.24284_24285delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297350.9:c.400+70_400+71delinsAC MANE Select	ENSP00000297350.4:n.400+70_400+71delinsAC
ENST00000297350.8:c.400+70_400+71delinsAC	ENSP00000297350.4:n.400+70_400+71delinsAC
ENST00000517352.1:c.400+70_400+71delinsAC	ENSP00000427924.1:n.400+70_400+71delinsAC
NM_002546.3:c.400+70_400+71delinsAC	NP_002537.3:n.400+70_400+71delinsAC
NM_002546.4:c.400+70_400+71delinsAC MANE Select	NP_002537.3:n.400+70_400+71delinsAC