Canonical Allele Identifier: CA2781929025

Gene: TNFRSF11B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118932766_118932782del , CM000670.2:g.118932766_118932782del	GRCh38
NC_000008.10:g.119945005_119945021del , CM000670.1:g.119945005_119945021del	GRCh37
NC_000008.9:g.120014186_120014202del	NCBI36
NG_012202.1:g.24364_24380del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297350.9:c.400+150_400+166del MANE Select	ENSP00000297350.4:n.400+150_400+166del
ENST00000297350.8:c.400+150_400+166del	ENSP00000297350.4:n.400+150_400+166del
ENST00000517352.1:c.400+150_400+166del	ENSP00000427924.1:n.400+150_400+166del
NM_002546.3:c.400+150_400+166del	NP_002537.3:n.400+150_400+166del
NM_002546.4:c.400+150_400+166del MANE Select	NP_002537.3:n.400+150_400+166del