Canonical Allele Identifier: CA1328471106
Community Standard Title: NM_001387777.1(TNS1):c.3901T= (p.Trp1301=)
Gene: TNS1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_001387777.1:c.3901T= MANE Select NP_001374706.1:p.Trp1301=
ENST00000682258.1:c.3901T= MANE Select ENSP00000506917.1:p.Trp1301=
NM_001308022.1:c.3550T= NP_001294951.1:p.Trp1184=
NM_001308022.2:c.3550T= NP_001294951.1:p.Trp1184=
NM_001308023.1:c.3526T= NP_001294952.1:p.Trp1176=
NM_001308023.2:c.3526T= NP_001294952.1:p.Trp1176=
NM_022648.4:c.3589T= NP_072174.3:p.Trp1197=
NM_022648.5:c.3589T= NP_072174.3:p.Trp1197=
NM_022648.6:c.3589T= NP_072174.3:p.Trp1197=
NM_022648.7:c.3589T= NP_072174.3:p.Trp1197=
ENST00000171887.8:c.3589T= ENSP00000171887.4:p.Trp1197=
ENST00000419504.5:c.3550T= ENSP00000408724.1:p.Trp1184=
ENST00000419504.6:c.3550T= ENSP00000408724.1:p.Trp1184=
ENST00000430930.5:c.3526T= ENSP00000406016.1:p.Trp1176=
ENST00000446688.5:c.922T= ENSP00000394171.2:p.Trp308=
ENST00000611415.4:c.3550T= ENSP00000484271.1:p.Trp1184=
ENST00000615025.4:c.2479T= ENSP00000480559.1:p.Trp827=
ENST00000615025.5:c.3526T= ENSP00000480559.2:p.Trp1176=
ENST00000615025.6:c.3526T= ENSP00000480559.2:p.Trp1176=
ENST00000646520.1:c.3964T= ENSP00000493967.1:p.Trp1322=
ENST00000651849.1:c.3865T= ENSP00000498399.1:p.Trp1289=
ENST00000705226.1:c.3676T= ENSP00000516092.1:p.Trp1226=
XM_011511711.1:c.3940T= XP_011510013.1:p.Trp1314=
XM_011511712.1:c.3916T= XP_011510014.1:p.Trp1306=
XM_011511713.1:c.3901T= XP_011510015.1:p.Trp1301=
XM_011511714.1:c.3892T= XP_011510016.1:p.Trp1298=
XM_011511715.1:c.3877T= XP_011510017.1:p.Trp1293=
XM_011511716.1:c.3853T= XP_011510018.1:p.Trp1285=
XM_011511717.1:c.3724T= XP_011510019.1:p.Trp1242=
XM_011511718.1:c.3676T= XP_011510020.1:p.Trp1226=
XM_011511721.1:c.3940T= XP_011510023.1:p.Trp1314=
XM_011511722.1:c.3940T= XP_011510024.1:p.Trp1314=
XM_011511723.1:c.3526T= XP_011510025.1:p.Trp1176=
XM_011511723.2:c.3526T= XP_011510025.1:p.Trp1176=
XM_011511724.1:c.2806T= XP_011510026.1:p.Trp936=
XM_011511725.1:c.2761T= XP_011510027.1:p.Trp921=
XM_011511726.1:c.2308T= XP_011510028.1:p.Trp770=
XM_011511727.1:c.985T= XP_011510029.1:p.Trp329=
XM_011511728.1:c.922T= XP_011510030.1:p.Trp308=
XM_017004811.1:c.3808T= XP_016860300.1:p.Trp1270=
XM_017004812.1:c.3808T= XP_016860301.1:p.Trp1270=
XM_017004813.2:c.2938T= XP_016860302.1:p.Trp980=
XM_017004814.1:c.2440T= XP_016860303.1:p.Trp814=
XM_017004815.1:c.2440T= XP_016860304.1:p.Trp814=
XM_017004816.2:c.1162T= XP_016860305.1:p.Trp388=
XM_024453068.1:c.4024T= XP_024308836.1:p.Trp1342=
XM_024453069.1:c.3937T= XP_024308837.1:p.Trp1313=
XM_024453070.1:c.3892T= XP_024308838.1:p.Trp1298=
XM_024453071.1:c.3868T= XP_024308839.1:p.Trp1290=
XM_024453072.1:c.3856T= XP_024308840.1:p.Trp1286=
XM_024453073.1:c.3853T= XP_024308841.1:p.Trp1285=
XM_024453074.1:c.3829T= XP_024308842.1:p.Trp1277=
XM_024453075.1:c.3781T= XP_024308843.1:p.Trp1261=
XM_024453076.1:c.3742T= XP_024308844.1:p.Trp1248=
XM_024453077.1:c.3565T= XP_024308845.1:p.Trp1189=
XM_024453078.1:c.3808T= XP_024308846.1:p.Trp1270=
XM_024453079.1:c.4399T= XP_024308847.1:p.Trp1467=
XM_024453080.1:c.4219T= XP_024308848.1:p.Trp1407=
XM_024453081.1:c.4024T= XP_024308849.1:p.Trp1342=
XM_024453082.1:c.4024T= XP_024308850.1:p.Trp1342=
XM_024453083.1:c.3901T= XP_024308851.1:p.Trp1301=
XM_024453084.1:c.3589T= XP_024308852.1:p.Trp1197=
XR_923002.1:n.3994T=