Canonical Allele Identifier: CA1154007904

Gene: TNFRSF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12208379_12208380delinsCT , CM000663.2:g.12208379_12208380delinsCT	GRCh38
NC_000001.10:g.12268436_12268437delinsCT , CM000663.1:g.12268436_12268437delinsCT	GRCh37
NC_000001.9:g.12191023_12191024delinsCT	NCBI36
NG_029791.1:g.46377_46378delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.*1359_*1360delinsCT MANE Select	ENSP00000365435.3:n.*1359_*1360delinsCT
ENST00000376259.6:c.*1359_*1360delinsCT	ENSP00000365435.3:n.*1359_*1360delinsCT
ENST00000492361.1:n.2734_2735delinsCT
NM_001066.2:c.*1359_*1360delinsCT	NP_001057.1:n.*1359_*1360delinsCT
XM_011542060.1:c.*1359_*1360delinsCT	XP_011540362.1:n.*1359_*1360delinsCT
XM_011542061.1:c.*1359_*1360delinsCT	XP_011540363.1:n.*1359_*1360delinsCT
XM_011542062.1:c.2793_2794delinsCT	XP_011540364.1:n.2793_2794delinsCT
XM_011542063.1:c.*1359_*1360delinsCT	XP_011540365.1:n.*1359_*1360delinsCT
XM_011542060.2:c.*1359_*1360delinsCT	XP_011540362.1:n.*1359_*1360delinsCT
XM_011542063.2:c.*1359_*1360delinsCT	XP_011540365.1:n.*1359_*1360delinsCT
XM_017002214.1:c.*1359_*1360delinsCT	XP_016857703.1:n.*1359_*1360delinsCT
XM_017002215.1:c.*1359_*1360delinsCT	XP_016857704.1:n.*1359_*1360delinsCT
NM_001066.3:c.*1359_*1360delinsCT MANE Select	NP_001057.1:n.*1359_*1360delinsCT