Canonical Allele Identifier: CA2643342838

Gene: TNFRSF1B

Linked Data

• gnomAD v4: 1-12208754-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12208755del , CM000663.2:g.12208755del	GRCh38
NC_000001.10:g.12268812del , CM000663.1:g.12268812del	GRCh37
NC_000001.9:g.12191399del	NCBI36
NG_029791.1:g.46753del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.*1735del MANE Select	ENSP00000365435.3:n.*1735del
ENST00000376259.6:c.*1735del	ENSP00000365435.3:n.*1735del
ENST00000492361.1:n.3110del
NM_001066.2:c.*1735del	NP_001057.1:n.*1735del
XM_011542060.1:c.*1735del	XP_011540362.1:n.*1735del
XM_011542061.1:c.*1735del	XP_011540363.1:n.*1735del
XM_011542062.1:c.3169del	XP_011540364.1:n.3169del
XM_011542063.1:c.*1735del	XP_011540365.1:n.*1735del
XM_011542060.2:c.*1735del	XP_011540362.1:n.*1735del
XM_011542063.2:c.*1735del	XP_011540365.1:n.*1735del
XM_017002214.1:c.*1735del	XP_016857703.1:n.*1735del
XM_017002215.1:c.*1735del	XP_016857704.1:n.*1735del
NM_001066.3:c.*1735del MANE Select	NP_001057.1:n.*1735del