Canonical Allele Identifier: CA1770724857

Gene: TNFRSF10B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23034787_23034789delinsCCA , CM000670.2:g.23034787_23034789delinsCCA	GRCh38
NC_000008.10:g.22892300_22892302delinsCCA , CM000670.1:g.22892300_22892302delinsCCA	GRCh37
NC_000008.9:g.22948245_22948247delinsCCA	NCBI36
NG_012145.1:g.39399_39401delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276431.9:c.251-3917_251-3915delinsTGG MANE Select	ENSP00000276431.4:n.251-3917_251-3915delinsTGG
ENST00000276431.8:c.251-3917_251-3915delinsTGG	ENSP00000276431.4:n.251-3917_251-3915delinsTGG
ENST00000347739.3:c.251-3917_251-3915delinsTGG	ENSP00000317859.3:n.251-3917_251-3915delinsTGG
ENST00000519910.1:n.258-3917_258-3915delinsTGG
ENST00000523504.5:c.145-3917_145-3915delinsTGG	ENSP00000427999.1:n.145-3917_145-3915delinsTGG
NM_003842.4:c.251-3917_251-3915delinsTGG	NP_003833.4:n.251-3917_251-3915delinsTGG
NM_147187.2:c.251-3917_251-3915delinsTGG	NP_671716.2:n.251-3917_251-3915delinsTGG
NR_027140.1:n.438-3917_438-3915delinsTGG
XR_949500.1:n.544-3917_544-3915delinsTGG
NM_003842.5:c.251-3917_251-3915delinsTGG MANE Select	NP_003833.4:n.251-3917_251-3915delinsTGG
NM_147187.3:c.251-3917_251-3915delinsTGG	NP_671716.2:n.251-3917_251-3915delinsTGG
NR_027140.2:n.282-3917_282-3915delinsTGG