Canonical Allele Identifier: CA2568845957

Gene: TNFRSF11B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118939449_118939450del , CM000670.2:g.118939449_118939450del	GRCh38
NC_000008.10:g.119951688_119951689del , CM000670.1:g.119951688_119951689del	GRCh37
NC_000008.9:g.120020869_120020870del	NCBI36
NG_012202.1:g.17696_17697del

Transcript Alleles

HGVS	Amino-acid change
ENST00000297350.9:c.31-6149_31-6148del MANE Select	ENSP00000297350.4:n.31-6149_31-6148del
ENST00000297350.8:c.31-6149_31-6148del	ENSP00000297350.4:n.31-6149_31-6148del
ENST00000517352.1:c.31-6149_31-6148del	ENSP00000427924.1:n.31-6149_31-6148del
NM_002546.3:c.31-6149_31-6148del	NP_002537.3:n.31-6149_31-6148del
NM_002546.4:c.31-6149_31-6148del MANE Select	NP_002537.3:n.31-6149_31-6148del