Canonical Allele Identifier: CA2202043964
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2084356C= , CM000678.2:g.2084356C= GRCh38
NC_000016.9:g.2134357C= , CM000678.1:g.2134357C= GRCh37
NC_000016.8:g.2074358C= NCBI36
NG_005895.1:g.40051C= , LRG_487:g.40051C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*2483C= ENSP00000455997.2:n.*2483C=
ENST00000642206.2:c.3981C= ENSP00000495146.2:p.Pro1327=
ENST00000642365.2:c.4131C= ENSP00000495459.2:p.Pro1377=
ENST00000644417.2:c.*4514C= ENSP00000493912.2:n.*4514C=
ENST00000646464.2:c.*6883C= ENSP00000496610.2:n.*6883C=
ENST00000219476.9:c.4134C= MANE Select ENSP00000219476.3:p.Pro1378=
ENST00000350773.9:c.4065C= ENSP00000344383.4:p.Pro1355=
ENST00000401874.7:c.3933C= ENSP00000384468.2:p.Pro1311=
ENST00000568454.6:c.3966C= ENSP00000454487.1:p.Pro1322=
ENST00000569110.2:c.370C=
ENST00000569930.2:n.2016C=
ENST00000642365.1:c.2788C=
ENST00000642561.1:c.4005C= ENSP00000495099.1:p.Pro1335=
ENST00000642728.1:n.316C=
ENST00000642797.1:c.3936C= ENSP00000493846.1:p.Pro1312=
ENST00000642936.1:c.4002C= ENSP00000494514.1:p.Pro1334=
ENST00000643088.1:c.3933C= ENSP00000494747.1:p.Pro1311=
ENST00000643177.1:n.148C=
ENST00000643426.1:n.1782C=
ENST00000643946.1:c.4065C= ENSP00000495927.1:p.Pro1355=
ENST00000644043.1:c.4005C= ENSP00000496262.1:p.Pro1335=
ENST00000644329.1:c.3933C= ENSP00000496611.1:p.Pro1311=
ENST00000644335.1:c.3936C= ENSP00000496317.1:p.Pro1312=
ENST00000644399.1:c.4055C=
ENST00000645024.1:n.2218C=
ENST00000645186.1:c.377C=
ENST00000646388.1:c.4134C= ENSP00000495921.1:p.Pro1378=
ENST00000646634.1:n.2949C=
ENST00000646674.1:n.1386C=
ENST00000647042.1:n.1357C=
ENST00000647180.1:n.1247C=
ENST00000219476.7:c.4134C= ENSP00000219476.3:p.Pro1378=
ENST00000350773.8:c.4065C= ENSP00000344383.4:p.Pro1355=
ENST00000382538.10:c.3789C= ENSP00000371978.6:p.Pro1263=
ENST00000401874.6:c.3933C= ENSP00000384468.2:p.Pro1311=
ENST00000439117.6:c.*3301C= ENSP00000406980.2:n.*3301C=
ENST00000439673.6:c.3825C= ENSP00000399232.2:p.Pro1275=
ENST00000497886.5:n.1892C=
ENST00000568454.5:c.3966C= ENSP00000454487.1:p.Pro1322=
ENST00000569110.1:c.316C=
ENST00000569930.1:n.1249C=
NM_000548.3:c.4134C= , LRG_487t1:c.4134C= NP_000539.2:p.Pro1378=
NM_001077183.1:c.3933C= NP_001070651.1:p.Pro1311=
NM_001114382.1:c.4065C= NP_001107854.1:p.Pro1355=
XM_005255529.3:c.4005C= XP_005255586.2:p.Pro1335=
XM_005255531.3:c.3936C= XP_005255588.2:p.Pro1312=
XM_011522636.1:c.4188C= XP_011520938.1:p.Pro1396=
XM_011522637.1:c.4185C= XP_011520939.1:p.Pro1395=
XM_011522638.1:c.4077C= XP_011520940.1:p.Pro1359=
XM_011522639.1:c.4059C= XP_011520941.1:p.Pro1353=
XM_011522640.1:c.4056C= XP_011520942.1:p.Pro1352=
XM_011522641.1:c.3825C= XP_011520943.1:p.Pro1275=
NM_000548.4:c.4134C= NP_000539.2:p.Pro1378=
NM_001077183.2:c.3933C= NP_001070651.1:p.Pro1311=
NM_001114382.2:c.4065C= NP_001107854.1:p.Pro1355=
NM_001318827.1:c.3825C= NP_001305756.1:p.Pro1275=
NM_001318829.1:c.3789C= NP_001305758.1:p.Pro1263=
NM_001318831.1:c.3402C= NP_001305760.1:p.Pro1134=
NM_001318832.1:c.3966C= NP_001305761.1:p.Pro1322=
NM_001363528.1:c.3936C= NP_001350457.1:p.Pro1312=
NM_021055.2:c.4005C= NP_066399.2:p.Pro1335=
XM_005255531.4:c.3936C= XP_005255588.2:p.Pro1312=
XM_011522636.2:c.4188C= XP_011520938.1:p.Pro1396=
XM_011522637.2:c.4185C= XP_011520939.1:p.Pro1395=
XM_011522638.2:c.4350C= XP_011520940.2:p.Pro1450=
XM_011522639.2:c.4059C= XP_011520941.1:p.Pro1353=
XM_011522640.2:c.4056C= XP_011520942.1:p.Pro1352=
XM_017023615.1:c.4131C= XP_016879104.1:p.Pro1377=
XM_017023616.1:c.4002C= XP_016879105.1:p.Pro1334=
XM_017023617.1:c.4098C= XP_016879106.1:p.Pro1366=
XM_017023618.1:c.2844C= XP_016879107.1:p.Pro948=
XM_024450413.1:c.3933C= XP_024306181.1:p.Pro1311=
NM_000548.5:c.4134C= MANE Select NP_000539.2:p.Pro1378=
NM_001370404.1:c.4002C= NP_001357333.1:p.Pro1334=
NM_001370405.1:c.4005C= NP_001357334.1:p.Pro1335=
NM_001077183.3:c.3933C= NP_001070651.1:p.Pro1311=
NM_001114382.3:c.4065C= NP_001107854.1:p.Pro1355=
NM_001318827.2:c.3825C= NP_001305756.1:p.Pro1275=
NM_001318829.2:c.3789C= NP_001305758.1:p.Pro1263=
NM_001318831.2:c.3402C= NP_001305760.1:p.Pro1134=
NM_001318832.2:c.3966C= NP_001305761.1:p.Pro1322=
NM_001363528.2:c.3936C= NP_001350457.1:p.Pro1312=
NM_021055.3:c.4005C= NP_066399.2:p.Pro1335=