Canonical Allele Identifier: CA388221906

Gene: TNFSF11

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_003701.4:c.781A>T MANE Select	NP_003692.1:p.Thr261Ser
ENST00000398795.7:c.781A>T MANE Select	ENSP00000381775.3:p.Thr261Ser
NM_003701.3:c.781A>T	NP_003692.1:p.Thr261Ser
NM_033012.3:c.562A>T	NP_143026.1:p.Thr188Ser
NM_033012.4:c.562A>T	NP_143026.1:p.Thr188Ser
ENST00000239849.8:c.640A>T	ENSP00000239849.7:p.Thr214Ser
ENST00000358545.6:c.562A>T	ENSP00000351347.2:p.Thr188Ser
ENST00000398795.6:c.781A>T	ENSP00000381775.3:p.Thr261Ser
ENST00000405262.6:c.562A>T	ENSP00000384042.2:p.Thr188Ser
ENST00000544862.5:c.562A>T	ENSP00000444913.1:p.Thr188Ser
XM_011535280.1:c.562A>T	XP_011533582.1:p.Thr188Ser
XM_011535280.2:c.562A>T	XP_011533582.1:p.Thr188Ser
XM_017020802.1:c.619A>T	XP_016876291.1:p.Thr207Ser
XM_017020803.2:c.562A>T	XP_016876292.1:p.Thr188Ser