Canonical Allele Identifier: CA1154005517

Gene: TNFRSF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12202845_12202846delinsAC , CM000663.2:g.12202845_12202846delinsAC	GRCh38
NC_000001.10:g.12262902_12262903delinsAC , CM000663.1:g.12262902_12262903delinsAC	GRCh37
NC_000001.9:g.12185489_12185490delinsAC	NCBI36
NG_029791.1:g.40843_40844delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.1105+674_1105+675delinsAC MANE Select	ENSP00000365435.3:n.1105+674_1105+675delinsAC
ENST00000376259.6:c.1105+674_1105+675delinsAC	ENSP00000365435.3:n.1105+674_1105+675delinsAC
ENST00000492361.1:n.1094+674_1094+675delinsAC
NM_001066.2:c.1105+674_1105+675delinsAC	NP_001057.1:n.1105+674_1105+675delinsAC
XM_011542060.1:c.1171+273_1171+274delinsAC	XP_011540362.1:n.1171+273_1171+274delinsAC
XM_011542061.1:c.1171+273_1171+274delinsAC	XP_011540363.1:n.1171+273_1171+274delinsAC
XM_011542062.1:c.1150+273_1150+274delinsAC	XP_011540364.1:n.1150+273_1150+274delinsAC
XM_011542063.1:c.1105+674_1105+675delinsAC	XP_011540365.1:n.1105+674_1105+675delinsAC
XM_011542060.2:c.1171+273_1171+274delinsAC	XP_011540362.1:n.1171+273_1171+274delinsAC
XM_011542063.2:c.1105+674_1105+675delinsAC	XP_011540365.1:n.1105+674_1105+675delinsAC
XM_017002214.1:c.586+273_586+274delinsAC	XP_016857703.1:n.586+273_586+274delinsAC
XM_017002215.1:c.520+674_520+675delinsAC	XP_016857704.1:n.520+674_520+675delinsAC
NM_001066.3:c.1105+674_1105+675delinsAC MANE Select	NP_001057.1:n.1105+674_1105+675delinsAC