Canonical Allele Identifier: CA1770738899

Gene: TNFRSF10B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23044055A= , CM000670.2:g.23044055A=	GRCh38
NC_000008.10:g.22901568A= , CM000670.1:g.22901568A=	GRCh37
NC_000008.9:g.22957513A=	NCBI36
NG_012145.1:g.30133T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276431.9:c.145-812T= MANE Select	ENSP00000276431.4:n.145-812T=
ENST00000276431.8:c.145-812T=	ENSP00000276431.4:n.145-812T=
ENST00000347739.3:c.145-812T=	ENSP00000317859.3:n.145-812T=
ENST00000519028.1:n.273-812T=
ENST00000519910.1:n.152-812T=
ENST00000523504.5:c.145-13183T=	ENSP00000427999.1:n.145-13183T=
NM_003842.4:c.145-812T=	NP_003833.4:n.145-812T=
NM_147187.2:c.145-812T=	NP_671716.2:n.145-812T=
NR_027140.1:n.438-13183T=
XR_949500.1:n.438-812T=
NM_003842.5:c.145-812T= MANE Select	NP_003833.4:n.145-812T=
NM_147187.3:c.145-812T=	NP_671716.2:n.145-812T=
NR_027140.2:n.282-13183T=