Canonical Allele Identifier: CA2514160120

Gene: TNFRSF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192983_12192984del , CM000663.2:g.12192983_12192984del	GRCh38
NC_000001.10:g.12253040_12253041del , CM000663.1:g.12253040_12253041del	GRCh37
NC_000001.9:g.12175627_12175628del	NCBI36
NG_029791.1:g.30981_30982del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.672_673del MANE Select	ENSP00000365435.3:p.Gln225ThrfsTer27
ENST00000376259.6:c.672_673del	ENSP00000365435.3:p.Gln225ThrfsTer27
ENST00000489921.1:n.384_385del
ENST00000492361.1:n.661_662del
NM_001066.2:c.672_673del	NP_001057.1:p.Gln225ThrfsTer27
XM_011542060.1:c.672_673del	XP_011540362.1:p.Gln225ThrfsTer27
XM_011542061.1:c.672_673del	XP_011540363.1:p.Gln225ThrfsTer27
XM_011542062.1:c.651_652del	XP_011540364.1:p.Gln218ThrfsTer27
XM_011542063.1:c.672_673del	XP_011540365.1:p.Gln225ThrfsTer27
XM_011542060.2:c.672_673del	XP_011540362.1:p.Gln225ThrfsTer27
XM_011542063.2:c.672_673del	XP_011540365.1:p.Gln225ThrfsTer27
XM_017002211.1:c.672_673del	XP_016857700.1:p.Gln225ThrfsTer27
XM_017002214.1:c.87_88del	XP_016857703.1:p.Gln30ThrfsTer27
XM_017002215.1:c.87_88del	XP_016857704.1:p.Gln30ThrfsTer27
NM_001066.3:c.672_673del MANE Select	NP_001057.1:p.Gln225ThrfsTer27