Canonical Allele Identifier: CA2742495528

Gene: TNFRSF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12208280_12208282del , CM000663.2:g.12208280_12208282del	GRCh38
NC_000001.10:g.12268337_12268339del , CM000663.1:g.12268337_12268339del	GRCh37
NC_000001.9:g.12190924_12190926del	NCBI36
NG_029791.1:g.46278_46280del

Transcript Alleles

HGVS	Amino-acid change
ENST00000376259.7:c.*1260_*1262del MANE Select	ENSP00000365435.3:n.*1260_*1262del
ENST00000376259.6:c.*1260_*1262del	ENSP00000365435.3:n.*1260_*1262del
ENST00000492361.1:n.2635_2637del
NM_001066.2:c.*1260_*1262del	NP_001057.1:n.*1260_*1262del
XM_011542060.1:c.*1260_*1262del	XP_011540362.1:n.*1260_*1262del
XM_011542061.1:c.*1260_*1262del	XP_011540363.1:n.*1260_*1262del
XM_011542062.1:c.2694_2696del	XP_011540364.1:n.2694_2696del
XM_011542063.1:c.*1260_*1262del	XP_011540365.1:n.*1260_*1262del
XM_011542060.2:c.*1260_*1262del	XP_011540362.1:n.*1260_*1262del
XM_011542063.2:c.*1260_*1262del	XP_011540365.1:n.*1260_*1262del
XM_017002214.1:c.*1260_*1262del	XP_016857703.1:n.*1260_*1262del
XM_017002215.1:c.*1260_*1262del	XP_016857704.1:n.*1260_*1262del
NM_001066.3:c.*1260_*1262del MANE Select	NP_001057.1:n.*1260_*1262del