Canonical Allele Identifier: CA350518151
Community Standard Title: NM_001387777.1(TNS1):c.3901T>G (p.Trp1301Gly)
Gene: TNS1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_001387777.1:c.3901T>G MANE Select NP_001374706.1:p.Trp1301Gly
ENST00000682258.1:c.3901T>G MANE Select ENSP00000506917.1:p.Trp1301Gly
NM_001308022.1:c.3550T>G NP_001294951.1:p.Trp1184Gly
NM_001308022.2:c.3550T>G NP_001294951.1:p.Trp1184Gly
NM_001308023.1:c.3526T>G NP_001294952.1:p.Trp1176Gly
NM_001308023.2:c.3526T>G NP_001294952.1:p.Trp1176Gly
NM_022648.4:c.3589T>G NP_072174.3:p.Trp1197Gly
NM_022648.5:c.3589T>G NP_072174.3:p.Trp1197Gly
NM_022648.6:c.3589T>G NP_072174.3:p.Trp1197Gly
NM_022648.7:c.3589T>G NP_072174.3:p.Trp1197Gly
ENST00000171887.8:c.3589T>G ENSP00000171887.4:p.Trp1197Gly
ENST00000419504.5:c.3550T>G ENSP00000408724.1:p.Trp1184Gly
ENST00000419504.6:c.3550T>G ENSP00000408724.1:p.Trp1184Gly
ENST00000430930.5:c.3526T>G ENSP00000406016.1:p.Trp1176Gly
ENST00000446688.5:c.922T>G ENSP00000394171.2:p.Trp308Gly
ENST00000611415.4:c.3550T>G ENSP00000484271.1:p.Trp1184Gly
ENST00000615025.4:c.2479T>G ENSP00000480559.1:p.Trp827Gly
ENST00000615025.5:c.3526T>G ENSP00000480559.2:p.Trp1176Gly
ENST00000615025.6:c.3526T>G ENSP00000480559.2:p.Trp1176Gly
ENST00000646520.1:c.3964T>G ENSP00000493967.1:p.Trp1322Gly
ENST00000651849.1:c.3865T>G ENSP00000498399.1:p.Trp1289Gly
ENST00000705226.1:c.3676T>G ENSP00000516092.1:p.Trp1226Gly
XM_011511711.1:c.3940T>G XP_011510013.1:p.Trp1314Gly
XM_011511712.1:c.3916T>G XP_011510014.1:p.Trp1306Gly
XM_011511713.1:c.3901T>G XP_011510015.1:p.Trp1301Gly
XM_011511714.1:c.3892T>G XP_011510016.1:p.Trp1298Gly
XM_011511715.1:c.3877T>G XP_011510017.1:p.Trp1293Gly
XM_011511716.1:c.3853T>G XP_011510018.1:p.Trp1285Gly
XM_011511717.1:c.3724T>G XP_011510019.1:p.Trp1242Gly
XM_011511718.1:c.3676T>G XP_011510020.1:p.Trp1226Gly
XM_011511721.1:c.3940T>G XP_011510023.1:p.Trp1314Gly
XM_011511722.1:c.3940T>G XP_011510024.1:p.Trp1314Gly
XM_011511723.1:c.3526T>G XP_011510025.1:p.Trp1176Gly
XM_011511723.2:c.3526T>G XP_011510025.1:p.Trp1176Gly
XM_011511724.1:c.2806T>G XP_011510026.1:p.Trp936Gly
XM_011511725.1:c.2761T>G XP_011510027.1:p.Trp921Gly
XM_011511726.1:c.2308T>G XP_011510028.1:p.Trp770Gly
XM_011511727.1:c.985T>G XP_011510029.1:p.Trp329Gly
XM_011511728.1:c.922T>G XP_011510030.1:p.Trp308Gly
XM_017004811.1:c.3808T>G XP_016860300.1:p.Trp1270Gly
XM_017004812.1:c.3808T>G XP_016860301.1:p.Trp1270Gly
XM_017004813.2:c.2938T>G XP_016860302.1:p.Trp980Gly
XM_017004814.1:c.2440T>G XP_016860303.1:p.Trp814Gly
XM_017004815.1:c.2440T>G XP_016860304.1:p.Trp814Gly
XM_017004816.2:c.1162T>G XP_016860305.1:p.Trp388Gly
XM_024453068.1:c.4024T>G XP_024308836.1:p.Trp1342Gly
XM_024453069.1:c.3937T>G XP_024308837.1:p.Trp1313Gly
XM_024453070.1:c.3892T>G XP_024308838.1:p.Trp1298Gly
XM_024453071.1:c.3868T>G XP_024308839.1:p.Trp1290Gly
XM_024453072.1:c.3856T>G XP_024308840.1:p.Trp1286Gly
XM_024453073.1:c.3853T>G XP_024308841.1:p.Trp1285Gly
XM_024453074.1:c.3829T>G XP_024308842.1:p.Trp1277Gly
XM_024453075.1:c.3781T>G XP_024308843.1:p.Trp1261Gly
XM_024453076.1:c.3742T>G XP_024308844.1:p.Trp1248Gly
XM_024453077.1:c.3565T>G XP_024308845.1:p.Trp1189Gly
XM_024453078.1:c.3808T>G XP_024308846.1:p.Trp1270Gly
XM_024453079.1:c.4399T>G XP_024308847.1:p.Trp1467Gly
XM_024453080.1:c.4219T>G XP_024308848.1:p.Trp1407Gly
XM_024453081.1:c.4024T>G XP_024308849.1:p.Trp1342Gly
XM_024453082.1:c.4024T>G XP_024308850.1:p.Trp1342Gly
XM_024453083.1:c.3901T>G XP_024308851.1:p.Trp1301Gly
XM_024453084.1:c.3589T>G XP_024308852.1:p.Trp1197Gly
XR_923002.1:n.3994T>G