Canonical Allele Identifier: CA1770724718

Gene: TNFRSF10B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23034691_23034694delinsACTC , CM000670.2:g.23034691_23034694delinsACTC	GRCh38
NC_000008.10:g.22892204_22892207delinsACTC , CM000670.1:g.22892204_22892207delinsACTC	GRCh37
NC_000008.9:g.22948149_22948152delinsACTC	NCBI36
NG_012145.1:g.39494_39497delinsGAGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000276431.9:c.251-3822_251-3819delinsGAGT MANE Select	ENSP00000276431.4:n.251-3822_251-3819delinsGAGT
ENST00000276431.8:c.251-3822_251-3819delinsGAGT	ENSP00000276431.4:n.251-3822_251-3819delinsGAGT
ENST00000347739.3:c.251-3822_251-3819delinsGAGT	ENSP00000317859.3:n.251-3822_251-3819delinsGAGT
ENST00000519910.1:n.258-3822_258-3819delinsGAGT
ENST00000523504.5:c.145-3822_145-3819delinsGAGT	ENSP00000427999.1:n.145-3822_145-3819delinsGAGT
NM_003842.4:c.251-3822_251-3819delinsGAGT	NP_003833.4:n.251-3822_251-3819delinsGAGT
NM_147187.2:c.251-3822_251-3819delinsGAGT	NP_671716.2:n.251-3822_251-3819delinsGAGT
NR_027140.1:n.438-3822_438-3819delinsGAGT
XR_949500.1:n.544-3822_544-3819delinsGAGT
NM_003842.5:c.251-3822_251-3819delinsGAGT MANE Select	NP_003833.4:n.251-3822_251-3819delinsGAGT
NM_147187.3:c.251-3822_251-3819delinsGAGT	NP_671716.2:n.251-3822_251-3819delinsGAGT
NR_027140.2:n.282-3822_282-3819delinsGAGT