Canonical Allele Identifier: CA1154008044

Gene: TNFRSF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12208761_12208762delinsTA , CM000663.2:g.12208761_12208762delinsTA	GRCh38
NC_000001.10:g.12268818_12268819delinsTA , CM000663.1:g.12268818_12268819delinsTA	GRCh37
NC_000001.9:g.12191405_12191406delinsTA	NCBI36
NG_029791.1:g.46759_46760delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.*1741_*1742delinsTA MANE Select	ENSP00000365435.3:n.*1741_*1742delinsTA
ENST00000376259.6:c.*1741_*1742delinsTA	ENSP00000365435.3:n.*1741_*1742delinsTA
ENST00000492361.1:n.3116_3117delinsTA
NM_001066.2:c.*1741_*1742delinsTA	NP_001057.1:n.*1741_*1742delinsTA
XM_011542060.1:c.*1741_*1742delinsTA	XP_011540362.1:n.*1741_*1742delinsTA
XM_011542061.1:c.*1741_*1742delinsTA	XP_011540363.1:n.*1741_*1742delinsTA
XM_011542062.1:c.3175_3176delinsTA	XP_011540364.1:n.3175_3176delinsTA
XM_011542063.1:c.*1741_*1742delinsTA	XP_011540365.1:n.*1741_*1742delinsTA
XM_011542060.2:c.*1741_*1742delinsTA	XP_011540362.1:n.*1741_*1742delinsTA
XM_011542063.2:c.*1741_*1742delinsTA	XP_011540365.1:n.*1741_*1742delinsTA
XM_017002214.1:c.*1741_*1742delinsTA	XP_016857703.1:n.*1741_*1742delinsTA
XM_017002215.1:c.*1741_*1742delinsTA	XP_016857704.1:n.*1741_*1742delinsTA
NM_001066.3:c.*1741_*1742delinsTA MANE Select	NP_001057.1:n.*1741_*1742delinsTA