Canonical Allele Identifier: CA388221910

Gene: TNFSF11

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.42606746C>G , CM000675.2:g.42606746C>G	GRCh38
NC_000013.10:g.43180882C>G , CM000675.1:g.43180882C>G	GRCh37
NC_000013.9:g.42078882C>G	NCBI36
NG_008990.1:g.49011C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_003701.4:c.782C>G MANE Select	NP_003692.1:p.Thr261Ser
ENST00000398795.7:c.782C>G MANE Select	ENSP00000381775.3:p.Thr261Ser
NM_003701.3:c.782C>G	NP_003692.1:p.Thr261Ser
NM_033012.3:c.563C>G	NP_143026.1:p.Thr188Ser
NM_033012.4:c.563C>G	NP_143026.1:p.Thr188Ser
ENST00000239849.8:c.641C>G	ENSP00000239849.7:p.Thr214Ser
ENST00000358545.6:c.563C>G	ENSP00000351347.2:p.Thr188Ser
ENST00000398795.6:c.782C>G	ENSP00000381775.3:p.Thr261Ser
ENST00000405262.6:c.563C>G	ENSP00000384042.2:p.Thr188Ser
ENST00000544862.5:c.563C>G	ENSP00000444913.1:p.Thr188Ser
XM_011535280.1:c.563C>G	XP_011533582.1:p.Thr188Ser
XM_011535280.2:c.563C>G	XP_011533582.1:p.Thr188Ser
XM_017020802.1:c.620C>G	XP_016876291.1:p.Thr207Ser
XM_017020803.2:c.563C>G	XP_016876292.1:p.Thr188Ser