Canonical Allele Identifier: CA2643340370

Gene: TNFRSF1B

Linked Data

• gnomAD v4: 1-12192915-T-TCCACGTCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192920_12192928dup , CM000663.2:g.12192920_12192928dup	GRCh38
NC_000001.10:g.12252977_12252985dup , CM000663.1:g.12252977_12252985dup	GRCh37
NC_000001.9:g.12175564_12175572dup	NCBI36
NG_029791.1:g.30918_30926dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000376259.7:c.609_617dup MANE Select	ENSP00000365435.3:p.Thr206_Arg207insSerProThr
ENST00000376259.6:c.609_617dup	ENSP00000365435.3:p.Thr206_Arg207insSerProThr
ENST00000489921.1:n.321_329dup
ENST00000492361.1:n.598_606dup
NM_001066.2:c.609_617dup	NP_001057.1:p.Thr206_Arg207insSerProThr
XM_011542060.1:c.609_617dup	XP_011540362.1:p.Thr206_Arg207insSerProThr
XM_011542061.1:c.609_617dup	XP_011540363.1:p.Thr206_Arg207insSerProThr
XM_011542062.1:c.588_596dup	XP_011540364.1:p.Thr199_Arg200insSerProThr
XM_011542063.1:c.609_617dup	XP_011540365.1:p.Thr206_Arg207insSerProThr
XM_011542060.2:c.609_617dup	XP_011540362.1:p.Thr206_Arg207insSerProThr
XM_011542063.2:c.609_617dup	XP_011540365.1:p.Thr206_Arg207insSerProThr
XM_017002211.1:c.609_617dup	XP_016857700.1:p.Thr206_Arg207insSerProThr
XM_017002214.1:c.24_32dup	XP_016857703.1:p.Thr11_Arg12insSerProThr
XM_017002215.1:c.24_32dup	XP_016857704.1:p.Thr11_Arg12insSerProThr
NM_001066.3:c.609_617dup MANE Select	NP_001057.1:p.Thr206_Arg207insSerProThr