Canonical Allele Identifier: CA2838979534

Gene: TNFRSF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192930dup , CM000663.2:g.12192930dup	GRCh38
NC_000001.10:g.12252987dup , CM000663.1:g.12252987dup	GRCh37
NC_000001.9:g.12175574dup	NCBI36
NG_029791.1:g.30928dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.619dup MANE Select	ENSP00000365435.3:p.Arg207ProfsTer?
ENST00000376259.6:c.619dup	ENSP00000365435.3:p.Arg207ProfsTer?
ENST00000489921.1:n.331dup
ENST00000492361.1:n.608dup
NM_001066.2:c.619dup	NP_001057.1:p.Arg207ProfsTer?
XM_011542060.1:c.619dup	XP_011540362.1:p.Arg207ProfsTer?
XM_011542061.1:c.619dup	XP_011540363.1:p.Arg207ProfsTer?
XM_011542062.1:c.598dup	XP_011540364.1:p.Arg200ProfsTer?
XM_011542063.1:c.619dup	XP_011540365.1:p.Arg207ProfsTer?
XM_011542060.2:c.619dup	XP_011540362.1:p.Arg207ProfsTer?
XM_011542063.2:c.619dup	XP_011540365.1:p.Arg207ProfsTer?
XM_017002211.1:c.619dup	XP_016857700.1:p.Arg207ProfsTer?
XM_017002214.1:c.34dup	XP_016857703.1:p.Arg12ProfsTer?
XM_017002215.1:c.34dup	XP_016857704.1:p.Arg12ProfsTer?
NM_001066.3:c.619dup MANE Select	NP_001057.1:p.Arg207ProfsTer?