Canonical Allele Identifier: CA1111794401

Gene: TNFRSF10B

Linked Data

• dbSNP Id: rs1811979715
• gnomAD v3: 8-23034691-ACTC-A
• gnomAD v4: 8-23034691-ACTC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23034693_23034695del , CM000670.2:g.23034693_23034695del	GRCh38
NC_000008.10:g.22892206_22892208del , CM000670.1:g.22892206_22892208del	GRCh37
NC_000008.9:g.22948151_22948153del	NCBI36
NG_012145.1:g.39494_39496del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276431.9:c.251-3822_251-3820del MANE Select	ENSP00000276431.4:n.251-3822_251-3820del
ENST00000276431.8:c.251-3822_251-3820del	ENSP00000276431.4:n.251-3822_251-3820del
ENST00000347739.3:c.251-3822_251-3820del	ENSP00000317859.3:n.251-3822_251-3820del
ENST00000519910.1:n.258-3822_258-3820del
ENST00000523504.5:c.145-3822_145-3820del	ENSP00000427999.1:n.145-3822_145-3820del
NM_003842.4:c.251-3822_251-3820del	NP_003833.4:n.251-3822_251-3820del
NM_147187.2:c.251-3822_251-3820del	NP_671716.2:n.251-3822_251-3820del
NR_027140.1:n.438-3822_438-3820del
XR_949500.1:n.544-3822_544-3820del
NM_003842.5:c.251-3822_251-3820del MANE Select	NP_003833.4:n.251-3822_251-3820del
NM_147187.3:c.251-3822_251-3820del	NP_671716.2:n.251-3822_251-3820del
NR_027140.2:n.282-3822_282-3820del