Canonical Allele Identifier: CA2688356289

Gene: TNFRSF11B

Linked Data

• gnomAD v4: 8-118932832-T-TTTTGC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118932832_118932833insTTTGC , CM000670.2:g.118932832_118932833insTTTGC	GRCh38
NC_000008.10:g.119945071_119945072insTTTGC , CM000670.1:g.119945071_119945072insTTTGC	GRCh37
NC_000008.9:g.120014252_120014253insTTTGC	NCBI36
NG_012202.1:g.24312_24313insGCAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297350.9:c.400+98_400+99insGCAAA MANE Select	ENSP00000297350.4:n.400+98_400+99insGCAAA
ENST00000297350.8:c.400+98_400+99insGCAAA	ENSP00000297350.4:n.400+98_400+99insGCAAA
ENST00000517352.1:c.400+98_400+99insGCAAA	ENSP00000427924.1:n.400+98_400+99insGCAAA
NM_002546.3:c.400+98_400+99insGCAAA	NP_002537.3:n.400+98_400+99insGCAAA
NM_002546.4:c.400+98_400+99insGCAAA MANE Select	NP_002537.3:n.400+98_400+99insGCAAA