Canonical Allele Identifier: CA2087386278

Gene: TNFSF11

Linked Data

• dbSNP Id: rs1873924484

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.42586865_42586866del , CM000675.2:g.42586865_42586866del	GRCh38
NC_000013.10:g.43161001_43161002del , CM000675.1:g.43161001_43161002del	GRCh37
NC_000013.9:g.42059001_42059002del	NCBI36
NG_008990.1:g.29130_29131del

Transcript Alleles

HGVS	Amino-acid change
ENST00000398795.7:c.387+5572_387+5573del MANE Select	ENSP00000381775.3:n.387+5572_387+5573del
ENST00000239849.8:c.246+5572_246+5573del	ENSP00000239849.7:n.246+5572_246+5573del
ENST00000358545.6:c.168+5572_168+5573del	ENSP00000351347.2:n.168+5572_168+5573del
ENST00000398795.6:c.387+5572_387+5573del	ENSP00000381775.3:n.387+5572_387+5573del
ENST00000405262.6:c.168+5572_168+5573del	ENSP00000384042.2:n.168+5572_168+5573del
ENST00000544862.5:c.168+5572_168+5573del	ENSP00000444913.1:n.168+5572_168+5573del
NM_003701.3:c.387+5572_387+5573del	NP_003692.1:n.387+5572_387+5573del
NM_033012.3:c.168+5572_168+5573del	NP_143026.1:n.168+5572_168+5573del
XM_011535280.1:c.168+5572_168+5573del	XP_011533582.1:n.168+5572_168+5573del
XM_011535280.2:c.168+5572_168+5573del	XP_011533582.1:n.168+5572_168+5573del
XM_017020802.1:c.225+5572_225+5573del	XP_016876291.1:n.225+5572_225+5573del
XM_017020803.2:c.168+5572_168+5573del	XP_016876292.1:n.168+5572_168+5573del
NM_003701.4:c.387+5572_387+5573del MANE Select	NP_003692.1:n.387+5572_387+5573del
NM_033012.4:c.168+5572_168+5573del	NP_143026.1:n.168+5572_168+5573del