Canonical Allele Identifier: CA049568
Community Standard Title: NM_000548.5(TSC2):c.3911G>T (p.Ser1304Ile)
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2083722G>T , CM000678.2:g.2083722G>T GRCh38
NC_000016.9:g.2133723G>T , CM000678.1:g.2133723G>T GRCh37
NC_000016.8:g.2073724G>T NCBI36
NG_005895.1:g.39417G>T , LRG_487:g.39417G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000548.5:c.3911G>T MANE Select NP_000539.2:p.Ser1304Ile
ENST00000219476.9:c.3911G>T MANE Select ENSP00000219476.3:p.Ser1304Ile
NM_000548.3:c.3911G>T , LRG_487t1:c.3911G>T NP_000539.2:p.Ser1304Ile
NM_000548.4:c.3911G>T NP_000539.2:p.Ser1304Ile
NM_001077183.1:c.3710G>T NP_001070651.1:p.Ser1237Ile
NM_001077183.2:c.3710G>T NP_001070651.1:p.Ser1237Ile
NM_001077183.3:c.3710G>T NP_001070651.1:p.Ser1237Ile
NM_001114382.1:c.3842G>T NP_001107854.1:p.Ser1281Ile
NM_001114382.2:c.3842G>T NP_001107854.1:p.Ser1281Ile
NM_001114382.3:c.3842G>T NP_001107854.1:p.Ser1281Ile
NM_001318827.1:c.3602G>T NP_001305756.1:p.Ser1201Ile
NM_001318827.2:c.3602G>T NP_001305756.1:p.Ser1201Ile
NM_001318829.1:c.3566G>T NP_001305758.1:p.Ser1189Ile
NM_001318829.2:c.3566G>T NP_001305758.1:p.Ser1189Ile
NM_001318831.1:c.3179G>T NP_001305760.1:p.Ser1060Ile
NM_001318831.2:c.3179G>T NP_001305760.1:p.Ser1060Ile
NM_001318832.1:c.3743G>T NP_001305761.1:p.Ser1248Ile
NM_001318832.2:c.3743G>T NP_001305761.1:p.Ser1248Ile
NM_001363528.1:c.3713G>T NP_001350457.1:p.Ser1238Ile
NM_001363528.2:c.3713G>T NP_001350457.1:p.Ser1238Ile
NM_001370404.1:c.3779G>T NP_001357333.1:p.Ser1260Ile
NM_001370405.1:c.3782G>T NP_001357334.1:p.Ser1261Ile
NM_021055.2:c.3782G>T NP_066399.2:p.Ser1261Ile
NM_021055.3:c.3782G>T NP_066399.2:p.Ser1261Ile
ENST00000219476.7:c.3911G>T ENSP00000219476.3:p.Ser1304Ile
ENST00000350773.8:c.3842G>T ENSP00000344383.4:p.Ser1281Ile
ENST00000350773.9:c.3842G>T ENSP00000344383.4:p.Ser1281Ile
ENST00000382538.10:c.3566G>T ENSP00000371978.6:p.Ser1189Ile
ENST00000401874.6:c.3710G>T ENSP00000384468.2:p.Ser1237Ile
ENST00000401874.7:c.3710G>T ENSP00000384468.2:p.Ser1237Ile
ENST00000439117.6:c.*3078G>T ENSP00000406980.2:n.*3078G>T
ENST00000439673.6:c.3602G>T ENSP00000399232.2:p.Ser1201Ile
ENST00000497886.5:n.1669G>T
ENST00000568454.5:c.3743G>T ENSP00000454487.1:p.Ser1248Ile
ENST00000568454.6:c.3743G>T ENSP00000454487.1:p.Ser1248Ile
ENST00000568566.6:c.*2260G>T ENSP00000455997.2:n.*2260G>T
ENST00000569110.1:c.93G>T
ENST00000569110.2:c.147G>T
ENST00000569930.1:n.1026G>T
ENST00000569930.2:n.1793G>T
ENST00000642206.2:c.3758G>T ENSP00000495146.2:p.Ser1253Ile
ENST00000642365.1:c.2565G>T
ENST00000642365.2:c.3908G>T ENSP00000495459.2:p.Ser1303Ile
ENST00000642561.1:c.3782G>T ENSP00000495099.1:p.Ser1261Ile
ENST00000642728.1:n.93G>T
ENST00000642797.1:c.3713G>T ENSP00000493846.1:p.Ser1238Ile
ENST00000642936.1:c.3779G>T ENSP00000494514.1:p.Ser1260Ile
ENST00000643088.1:c.3710G>T ENSP00000494747.1:p.Ser1237Ile
ENST00000643426.1:n.1559G>T
ENST00000643533.1:n.352G>T
ENST00000643946.1:c.3842G>T ENSP00000495927.1:p.Ser1281Ile
ENST00000644043.1:c.3782G>T ENSP00000496262.1:p.Ser1261Ile
ENST00000644329.1:c.3710G>T ENSP00000496611.1:p.Ser1237Ile
ENST00000644335.1:c.3713G>T ENSP00000496317.1:p.Ser1238Ile
ENST00000644399.1:c.3832G>T
ENST00000644417.2:c.*4291G>T ENSP00000493912.2:n.*4291G>T
ENST00000645024.1:n.1995G>T
ENST00000645186.1:c.154G>T
ENST00000646388.1:c.3911G>T ENSP00000495921.1:p.Ser1304Ile
ENST00000646464.2:c.*6660G>T ENSP00000496610.2:n.*6660G>T
ENST00000646634.1:n.2726G>T
ENST00000646674.1:n.1163G>T
ENST00000647042.1:n.1134G>T
ENST00000647180.1:n.1024G>T
XM_005255529.3:c.3782G>T XP_005255586.2:p.Ser1261Ile
XM_005255531.3:c.3713G>T XP_005255588.2:p.Ser1238Ile
XM_005255531.4:c.3713G>T XP_005255588.2:p.Ser1238Ile
XM_011522636.1:c.3965G>T XP_011520938.1:p.Ser1322Ile
XM_011522636.2:c.3965G>T XP_011520938.1:p.Ser1322Ile
XM_011522637.1:c.3962G>T XP_011520939.1:p.Ser1321Ile
XM_011522637.2:c.3962G>T XP_011520939.1:p.Ser1321Ile
XM_011522638.1:c.3854G>T XP_011520940.1:p.Ser1285Ile
XM_011522638.2:c.4127G>T XP_011520940.2:p.Ser1376Ile
XM_011522639.1:c.3836G>T XP_011520941.1:p.Ser1279Ile
XM_011522639.2:c.3836G>T XP_011520941.1:p.Ser1279Ile
XM_011522640.1:c.3833G>T XP_011520942.1:p.Ser1278Ile
XM_011522640.2:c.3833G>T XP_011520942.1:p.Ser1278Ile
XM_011522641.1:c.3602G>T XP_011520943.1:p.Ser1201Ile
XM_017023615.1:c.3908G>T XP_016879104.1:p.Ser1303Ile
XM_017023616.1:c.3779G>T XP_016879105.1:p.Ser1260Ile
XM_017023617.1:c.3875G>T XP_016879106.1:p.Ser1292Ile
XM_017023618.1:c.2621G>T XP_016879107.1:p.Ser874Ile
XM_024450413.1:c.3710G>T XP_024306181.1:p.Ser1237Ile