Canonical Allele Identifier: CA249053404

Gene: TNFSF11

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.42606745A>G , CM000675.2:g.42606745A>G	GRCh38
NC_000013.10:g.43180881A>G , CM000675.1:g.43180881A>G	GRCh37
NC_000013.9:g.42078881A>G	NCBI36
NG_008990.1:g.49010A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398795.7:c.781A>G MANE Select	ENSP00000381775.3:p.Thr261Ala
ENST00000239849.8:c.640A>G	ENSP00000239849.7:p.Thr214Ala
ENST00000358545.6:c.562A>G	ENSP00000351347.2:p.Thr188Ala
ENST00000398795.6:c.781A>G	ENSP00000381775.3:p.Thr261Ala
ENST00000405262.6:c.562A>G	ENSP00000384042.2:p.Thr188Ala
ENST00000544862.5:c.562A>G	ENSP00000444913.1:p.Thr188Ala
NM_003701.3:c.781A>G	NP_003692.1:p.Thr261Ala
NM_033012.3:c.562A>G	NP_143026.1:p.Thr188Ala
XM_011535280.1:c.562A>G	XP_011533582.1:p.Thr188Ala
XM_011535280.2:c.562A>G	XP_011533582.1:p.Thr188Ala
XM_017020802.1:c.619A>G	XP_016876291.1:p.Thr207Ala
XM_017020803.2:c.562A>G	XP_016876292.1:p.Thr188Ala
NM_003701.4:c.781A>G MANE Select	NP_003692.1:p.Thr261Ala
NM_033012.4:c.562A>G	NP_143026.1:p.Thr188Ala