Canonical Allele Identifier: CA2099756

Gene: TNS1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.217818431A>G , CM000664.2:g.217818431A>G	GRCh38
NC_000002.11:g.218683154A>G , CM000664.1:g.218683154A>G	GRCh37
NC_000002.10:g.218391399A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419504.6:c.3550T>C	ENSP00000408724.1:p.Trp1184Arg
ENST00000615025.6:c.3526T>C	ENSP00000480559.2:p.Trp1176Arg
ENST00000705226.1:c.3676T>C	ENSP00000516092.1:p.Trp1226Arg
ENST00000615025.5:c.3526T>C	ENSP00000480559.2:p.Trp1176Arg
ENST00000682258.1:c.3901T>C MANE Select	ENSP00000506917.1:p.Trp1301Arg
ENST00000646520.1:c.3964T>C	ENSP00000493967.1:p.Trp1322Arg
ENST00000651849.1:c.3865T>C	ENSP00000498399.1:p.Trp1289Arg
ENST00000171887.8:c.3589T>C	ENSP00000171887.4:p.Trp1197Arg
ENST00000419504.5:c.3550T>C	ENSP00000408724.1:p.Trp1184Arg
ENST00000430930.5:c.3526T>C	ENSP00000406016.1:p.Trp1176Arg
ENST00000446688.5:c.922T>C	ENSP00000394171.2:p.Trp308Arg
ENST00000611415.4:c.3550T>C	ENSP00000484271.1:p.Trp1184Arg
ENST00000615025.4:c.2479T>C	ENSP00000480559.1:p.Trp827Arg
NM_001308022.1:c.3550T>C	NP_001294951.1:p.Trp1184Arg
NM_001308023.1:c.3526T>C	NP_001294952.1:p.Trp1176Arg
NM_022648.4:c.3589T>C	NP_072174.3:p.Trp1197Arg
NM_022648.5:c.3589T>C	NP_072174.3:p.Trp1197Arg
XM_011511711.1:c.3940T>C	XP_011510013.1:p.Trp1314Arg
XM_011511712.1:c.3916T>C	XP_011510014.1:p.Trp1306Arg
XM_011511713.1:c.3901T>C	XP_011510015.1:p.Trp1301Arg
XM_011511714.1:c.3892T>C	XP_011510016.1:p.Trp1298Arg
XM_011511715.1:c.3877T>C	XP_011510017.1:p.Trp1293Arg
XM_011511716.1:c.3853T>C	XP_011510018.1:p.Trp1285Arg
XM_011511717.1:c.3724T>C	XP_011510019.1:p.Trp1242Arg
XM_011511718.1:c.3676T>C	XP_011510020.1:p.Trp1226Arg
XM_011511721.1:c.3940T>C	XP_011510023.1:p.Trp1314Arg
XM_011511722.1:c.3940T>C	XP_011510024.1:p.Trp1314Arg
XM_011511723.1:c.3526T>C	XP_011510025.1:p.Trp1176Arg
XM_011511724.1:c.2806T>C	XP_011510026.1:p.Trp936Arg
XM_011511725.1:c.2761T>C	XP_011510027.1:p.Trp921Arg
XM_011511726.1:c.2308T>C	XP_011510028.1:p.Trp770Arg
XM_011511727.1:c.985T>C	XP_011510029.1:p.Trp329Arg
XM_011511728.1:c.922T>C	XP_011510030.1:p.Trp308Arg
XR_923002.1:n.3994T>C
XM_011511723.2:c.3526T>C	XP_011510025.1:p.Trp1176Arg
XM_017004811.1:c.3808T>C	XP_016860300.1:p.Trp1270Arg
XM_017004812.1:c.3808T>C	XP_016860301.1:p.Trp1270Arg
XM_017004813.2:c.2938T>C	XP_016860302.1:p.Trp980Arg
XM_017004814.1:c.2440T>C	XP_016860303.1:p.Trp814Arg
XM_017004815.1:c.2440T>C	XP_016860304.1:p.Trp814Arg
XM_017004816.2:c.1162T>C	XP_016860305.1:p.Trp388Arg
XM_024453068.1:c.4024T>C	XP_024308836.1:p.Trp1342Arg
XM_024453069.1:c.3937T>C	XP_024308837.1:p.Trp1313Arg
XM_024453070.1:c.3892T>C	XP_024308838.1:p.Trp1298Arg
XM_024453071.1:c.3868T>C	XP_024308839.1:p.Trp1290Arg
XM_024453072.1:c.3856T>C	XP_024308840.1:p.Trp1286Arg
XM_024453073.1:c.3853T>C	XP_024308841.1:p.Trp1285Arg
XM_024453074.1:c.3829T>C	XP_024308842.1:p.Trp1277Arg
XM_024453075.1:c.3781T>C	XP_024308843.1:p.Trp1261Arg
XM_024453076.1:c.3742T>C	XP_024308844.1:p.Trp1248Arg
XM_024453077.1:c.3565T>C	XP_024308845.1:p.Trp1189Arg
XM_024453078.1:c.3808T>C	XP_024308846.1:p.Trp1270Arg
XM_024453079.1:c.4399T>C	XP_024308847.1:p.Trp1467Arg
XM_024453080.1:c.4219T>C	XP_024308848.1:p.Trp1407Arg
XM_024453081.1:c.4024T>C	XP_024308849.1:p.Trp1342Arg
XM_024453082.1:c.4024T>C	XP_024308850.1:p.Trp1342Arg
XM_024453083.1:c.3901T>C	XP_024308851.1:p.Trp1301Arg
XM_024453084.1:c.3589T>C	XP_024308852.1:p.Trp1197Arg
NM_001308023.2:c.3526T>C	NP_001294952.1:p.Trp1176Arg
NM_022648.6:c.3589T>C	NP_072174.3:p.Trp1197Arg
NM_001308022.2:c.3550T>C	NP_001294951.1:p.Trp1184Arg
NM_001387777.1:c.3901T>C MANE Select	NP_001374706.1:p.Trp1301Arg
NM_022648.7:c.3589T>C	NP_072174.3:p.Trp1197Arg