Canonical Allele Identifier: CA2643342776

Gene: TNFRSF1B

Linked Data

• gnomAD v4: 1-12208642-A-AGATGACTGAGTCCTCGTAGCCATCTCTCTACTCCTACCTCAGCCTAGACCCTCC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12208642_12208643insGATGACTGAGTCCTCGTAGCCATCTCTCTACTCCTACCTCAGCCTAGACCCTCC , CM000663.2:g.12208642_12208643insGATGACTGAGTCCTCGTAGCCATCTCTCTACTCCTACCTCAGCCTAGACCCTCC	GRCh38
NC_000001.10:g.12268699_12268700insGATGACTGAGTCCTCGTAGCCATCTCTCTACTCCTACCTCAGCCTAGACCCTCC , CM000663.1:g.12268699_12268700insGATGACTGAGTCCTCGTAGCCATCTCTCTACTCCTACCTCAGCCTAGACCCTCC	GRCh37
NC_000001.9:g.12191286_12191287insGATGACTGAGTCCTCGTAGCCATCTCTCTACTCCTACCTCAGCCTAGACCCTCC	NCBI36
NG_029791.1:g.46640_46641insGATGACTGAGTCCTCGTAGCCATCTCTCTACTCCTACCTCAGCCTAGACCCTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.*1622_*1623insGATGACTGAGTCCTCGTAGCCATCTCTCTACTCCTACCTCAGCCTAGACCCTCC MANE Select	ENSP00000365435.3:n.*1622_*1623insGATGACTGAGTCCTCGTAGCCATCTCT...
ENST00000376259.6:c.*1622_*1623insGATGACTGAGTCCTCGTAGCCATCTCTCTACTCCTACCTCAGCCTAGACCCTCC	ENSP00000365435.3:n.*1622_*1623insGATGACTGAGTCCTCGTAGCCATCTCT...
ENST00000492361.1:n.2997_2998insGATGACTGAGTCCTCGTAGCCATCTCTCTACTCCTACCTCAGCCTAGACCCTCC
NM_001066.2:c.*1622_*1623insGATGACTGAGTCCTCGTAGCCATCTCTCTACTCCTACCTCAGCCTAGACCCTCC	NP_001057.1:n.*1622_*1623insGATGACTGAGTCCTCGTAGCCATCTCTCTACTC...
XM_011542060.1:c.*1622_*1623insGATGACTGAGTCCTCGTAGCCATCTCTCTACTCCTACCTCAGCCTAGACCCTCC	XP_011540362.1:n.*1622_*1623insGATGACTGAGTCCTCGTAGCCATCTCTCTA...
XM_011542061.1:c.*1622_*1623insGATGACTGAGTCCTCGTAGCCATCTCTCTACTCCTACCTCAGCCTAGACCCTCC	XP_011540363.1:n.*1622_*1623insGATGACTGAGTCCTCGTAGCCATCTCTCTA...
XM_011542062.1:c.3056_3057insGATGACTGAGTCCTCGTAGCCATCTCTCTACTCCTACCTCAGCCTAGACCCTCC	XP_011540364.1:n.3056_3057insGATGACTGAGTCCTCGTAGCCATCTCTCTACT...
XM_011542063.1:c.*1622_*1623insGATGACTGAGTCCTCGTAGCCATCTCTCTACTCCTACCTCAGCCTAGACCCTCC	XP_011540365.1:n.*1622_*1623insGATGACTGAGTCCTCGTAGCCATCTCTCTA...
XM_011542060.2:c.*1622_*1623insGATGACTGAGTCCTCGTAGCCATCTCTCTACTCCTACCTCAGCCTAGACCCTCC	XP_011540362.1:n.*1622_*1623insGATGACTGAGTCCTCGTAGCCATCTCTCTA...
XM_011542063.2:c.*1622_*1623insGATGACTGAGTCCTCGTAGCCATCTCTCTACTCCTACCTCAGCCTAGACCCTCC	XP_011540365.1:n.*1622_*1623insGATGACTGAGTCCTCGTAGCCATCTCTCTA...
XM_017002214.1:c.*1622_*1623insGATGACTGAGTCCTCGTAGCCATCTCTCTACTCCTACCTCAGCCTAGACCCTCC	XP_016857703.1:n.*1622_*1623insGATGACTGAGTCCTCGTAGCCATCTCTCTA...
XM_017002215.1:c.*1622_*1623insGATGACTGAGTCCTCGTAGCCATCTCTCTACTCCTACCTCAGCCTAGACCCTCC	XP_016857704.1:n.*1622_*1623insGATGACTGAGTCCTCGTAGCCATCTCTCTA...
NM_001066.3:c.*1622_*1623insGATGACTGAGTCCTCGTAGCCATCTCTCTACTCCTACCTCAGCCTAGACCCTCC MANE Select	NP_001057.1:n.*1622_*1623insGATGACTGAGTCCTCGTAGCCATCTCTCTACTC...