Canonical Allele Identifier: CA2839538235

Gene: TNFRSF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12193024dup , CM000663.2:g.12193024dup	GRCh38
NC_000001.10:g.12253081dup , CM000663.1:g.12253081dup	GRCh37
NC_000001.9:g.12175668dup	NCBI36
NG_029791.1:g.31022dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.713dup MANE Select	ENSP00000365435.3:p.Ser238ArgfsTer15
ENST00000376259.6:c.713dup	ENSP00000365435.3:p.Ser238ArgfsTer15
ENST00000492361.1:n.702dup
NM_001066.2:c.713dup	NP_001057.1:p.Ser238ArgfsTer15
XM_011542060.1:c.713dup	XP_011540362.1:p.Ser238ArgfsTer15
XM_011542061.1:c.713dup	XP_011540363.1:p.Ser238ArgfsTer15
XM_011542062.1:c.692dup	XP_011540364.1:p.Ser231ArgfsTer15
XM_011542063.1:c.713dup	XP_011540365.1:p.Ser238ArgfsTer15
XM_011542060.2:c.713dup	XP_011540362.1:p.Ser238ArgfsTer15
XM_011542063.2:c.713dup	XP_011540365.1:p.Ser238ArgfsTer15
XM_017002211.1:c.713dup	XP_016857700.1:p.Ser238ArgfsTer15
XM_017002214.1:c.128dup	XP_016857703.1:p.Ser43ArgfsTer15
XM_017002215.1:c.128dup	XP_016857704.1:p.Ser43ArgfsTer15
NM_001066.3:c.713dup MANE Select	NP_001057.1:p.Ser238ArgfsTer15