Canonical Allele Identifier: CA1154001412

Gene: TNFRSF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192869_12192872delinsCGTG , CM000663.2:g.12192869_12192872delinsCGTG	GRCh38
NC_000001.10:g.12252926_12252929delinsCGTG , CM000663.1:g.12252926_12252929delinsCGTG	GRCh37
NC_000001.9:g.12175513_12175516delinsCGTG	NCBI36
NG_029791.1:g.30867_30870delinsCGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.558_561delinsCGTG MANE Select	ENSP00000365435.3:p.Asn186=
ENST00000376259.6:c.558_561delinsCGTG	ENSP00000365435.3:p.Asn186=
ENST00000489921.1:n.270_273delinsCGTG
ENST00000492361.1:n.547_550delinsCGTG
NM_001066.2:c.558_561delinsCGTG	NP_001057.1:p.Asn186=
XM_011542060.1:c.558_561delinsCGTG	XP_011540362.1:p.Asn186=
XM_011542061.1:c.558_561delinsCGTG	XP_011540363.1:p.Asn186=
XM_011542062.1:c.537_540delinsCGTG	XP_011540364.1:p.Asn179=
XM_011542063.1:c.558_561delinsCGTG	XP_011540365.1:p.Asn186=
XM_011542060.2:c.558_561delinsCGTG	XP_011540362.1:p.Asn186=
XM_011542063.2:c.558_561delinsCGTG	XP_011540365.1:p.Asn186=
XM_017002211.1:c.558_561delinsCGTG	XP_016857700.1:p.Asn186=
XM_017002214.1:c.-28_-25delinsCGTG	XP_016857703.1:n.-28_-25delinsCGTG
XM_017002215.1:c.-28_-25delinsCGTG	XP_016857704.1:n.-28_-25delinsCGTG
NM_001066.3:c.558_561delinsCGTG MANE Select	NP_001057.1:p.Asn186=