Canonical Allele Identifier: CA1814482848

Gene: TNFRSF11B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118947723_118947726delinsTAGA , CM000670.2:g.118947723_118947726delinsTAGA	GRCh38
NC_000008.10:g.119959962_119959965delinsTAGA , CM000670.1:g.119959962_119959965delinsTAGA	GRCh37
NC_000008.9:g.120029143_120029146delinsTAGA	NCBI36
NG_012202.1:g.9419_9422delinsTCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297350.9:c.30+4066_30+4069delinsTCTA MANE Select	ENSP00000297350.4:n.30+4066_30+4069delinsTCTA
ENST00000297350.8:c.30+4066_30+4069delinsTCTA	ENSP00000297350.4:n.30+4066_30+4069delinsTCTA
ENST00000517352.1:c.30+4066_30+4069delinsTCTA	ENSP00000427924.1:n.30+4066_30+4069delinsTCTA
NM_002546.3:c.30+4066_30+4069delinsTCTA	NP_002537.3:n.30+4066_30+4069delinsTCTA
NM_002546.4:c.30+4066_30+4069delinsTCTA MANE Select	NP_002537.3:n.30+4066_30+4069delinsTCTA