Canonical Allele Identifier: CA2999388462

Gene: TSC2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2084554dup , CM000678.2:g.2084554dup	GRCh38
NC_000016.9:g.2134555dup , CM000678.1:g.2134555dup	GRCh37
NC_000016.8:g.2074556dup	NCBI36
NG_005895.1:g.40249dup , LRG_487:g.40249dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*2681dup	ENSP00000455997.2:n.*2681dup
ENST00000642206.2:c.4179dup	ENSP00000495146.2:p.Pro1395AlafsTer?
ENST00000642365.2:c.4329dup	ENSP00000495459.2:p.Pro1445AlafsTer?
ENST00000644417.2:c.*4712dup	ENSP00000493912.2:n.*4712dup
ENST00000646464.2:c.*7081dup	ENSP00000496610.2:n.*7081dup
ENST00000219476.9:c.4332dup MANE Select	ENSP00000219476.3:p.Pro1446AlafsTer?
ENST00000350773.9:c.4263dup	ENSP00000344383.4:p.Pro1423AlafsTer?
ENST00000401874.7:c.4131dup	ENSP00000384468.2:p.Pro1379AlafsTer?
ENST00000568454.6:c.4164dup	ENSP00000454487.1:p.Pro1390AlafsTer?
ENST00000569110.2:c.568dup
ENST00000569930.2:n.2214dup
ENST00000642365.1:c.2986dup
ENST00000642561.1:c.4203dup	ENSP00000495099.1:p.Pro1403AlafsTer?
ENST00000642728.1:n.514dup
ENST00000642797.1:c.4134dup	ENSP00000493846.1:p.Pro1380AlafsTer?
ENST00000642936.1:c.4200dup	ENSP00000494514.1:p.Pro1402AlafsTer?
ENST00000643088.1:c.4131dup	ENSP00000494747.1:p.Pro1379AlafsTer?
ENST00000643177.1:n.346dup
ENST00000643426.1:n.1980dup
ENST00000643946.1:c.4263dup	ENSP00000495927.1:p.Pro1423AlafsTer?
ENST00000644043.1:c.4203dup	ENSP00000496262.1:p.Pro1403AlafsTer?
ENST00000644329.1:c.4131dup	ENSP00000496611.1:p.Pro1379AlafsTer?
ENST00000644335.1:c.4134dup	ENSP00000496317.1:p.Pro1380AlafsTer?
ENST00000644399.1:c.4253dup
ENST00000645024.1:n.2416dup
ENST00000646388.1:c.4332dup	ENSP00000495921.1:p.Pro1446AlafsTer?
ENST00000646634.1:n.3147dup
ENST00000646674.1:n.1584dup
ENST00000647042.1:n.1555dup
ENST00000647180.1:n.1445dup
ENST00000219476.7:c.4332dup	ENSP00000219476.3:p.Pro1446AlafsTer?
ENST00000350773.8:c.4263dup	ENSP00000344383.4:p.Pro1423AlafsTer?
ENST00000382538.10:c.3987dup	ENSP00000371978.6:p.Pro1331AlafsTer?
ENST00000401874.6:c.4131dup	ENSP00000384468.2:p.Pro1379AlafsTer?
ENST00000439117.6:c.*3499dup	ENSP00000406980.2:n.*3499dup
ENST00000439673.6:c.4023dup	ENSP00000399232.2:p.Pro1343AlafsTer?
ENST00000497886.5:n.2090dup
ENST00000568454.5:c.4164dup	ENSP00000454487.1:p.Pro1390AlafsTer?
ENST00000569110.1:c.514dup
ENST00000569930.1:n.1447dup
NM_000548.3:c.4332dup , LRG_487t1:c.4332dup	NP_000539.2:p.Pro1446AlafsTer?
NM_001077183.1:c.4131dup	NP_001070651.1:p.Pro1379AlafsTer?
NM_001114382.1:c.4263dup	NP_001107854.1:p.Pro1423AlafsTer?
XM_005255529.3:c.4203dup	XP_005255586.2:p.Pro1403AlafsTer?
XM_005255531.3:c.4134dup	XP_005255588.2:p.Pro1380AlafsTer?
XM_011522636.1:c.4386dup	XP_011520938.1:p.Pro1464AlafsTer?
XM_011522637.1:c.4383dup	XP_011520939.1:p.Pro1463AlafsTer?
XM_011522638.1:c.4275dup	XP_011520940.1:p.Pro1427AlafsTer?
XM_011522639.1:c.4257dup	XP_011520941.1:p.Pro1421AlafsTer?
XM_011522640.1:c.4254dup	XP_011520942.1:p.Pro1420AlafsTer?
XM_011522641.1:c.4023dup	XP_011520943.1:p.Pro1343AlafsTer?
NM_000548.4:c.4332dup	NP_000539.2:p.Pro1446AlafsTer?
NM_001077183.2:c.4131dup	NP_001070651.1:p.Pro1379AlafsTer?
NM_001114382.2:c.4263dup	NP_001107854.1:p.Pro1423AlafsTer?
NM_001318827.1:c.4023dup	NP_001305756.1:p.Pro1343AlafsTer?
NM_001318829.1:c.3987dup	NP_001305758.1:p.Pro1331AlafsTer?
NM_001318831.1:c.3600dup	NP_001305760.1:p.Pro1202AlafsTer?
NM_001318832.1:c.4164dup	NP_001305761.1:p.Pro1390AlafsTer?
NM_001363528.1:c.4134dup	NP_001350457.1:p.Pro1380AlafsTer?
NM_021055.2:c.4203dup	NP_066399.2:p.Pro1403AlafsTer?
XM_005255531.4:c.4134dup	XP_005255588.2:p.Pro1380AlafsTer?
XM_011522636.2:c.4386dup	XP_011520938.1:p.Pro1464AlafsTer?
XM_011522637.2:c.4383dup	XP_011520939.1:p.Pro1463AlafsTer?
XM_011522638.2:c.4548dup	XP_011520940.2:p.Pro1518AlafsTer?
XM_011522639.2:c.4257dup	XP_011520941.1:p.Pro1421AlafsTer?
XM_011522640.2:c.4254dup	XP_011520942.1:p.Pro1420AlafsTer?
XM_017023615.1:c.4329dup	XP_016879104.1:p.Pro1445AlafsTer?
XM_017023616.1:c.4200dup	XP_016879105.1:p.Pro1402AlafsTer?
XM_017023617.1:c.4296dup	XP_016879106.1:p.Pro1434AlafsTer?
XM_017023618.1:c.3042dup	XP_016879107.1:p.Pro1016AlafsTer?
XM_024450413.1:c.4131dup	XP_024306181.1:p.Pro1379AlafsTer?
NM_000548.5:c.4332dup MANE Select	NP_000539.2:p.Pro1446AlafsTer?
NM_001370404.1:c.4200dup	NP_001357333.1:p.Pro1402AlafsTer?
NM_001370405.1:c.4203dup	NP_001357334.1:p.Pro1403AlafsTer?
NM_001077183.3:c.4131dup	NP_001070651.1:p.Pro1379AlafsTer?
NM_001114382.3:c.4263dup	NP_001107854.1:p.Pro1423AlafsTer?
NM_001318827.2:c.4023dup	NP_001305756.1:p.Pro1343AlafsTer?
NM_001318829.2:c.3987dup	NP_001305758.1:p.Pro1331AlafsTer?
NM_001318831.2:c.3600dup	NP_001305760.1:p.Pro1202AlafsTer?
NM_001318832.2:c.4164dup	NP_001305761.1:p.Pro1390AlafsTer?
NM_001363528.2:c.4134dup	NP_001350457.1:p.Pro1380AlafsTer?
NM_021055.3:c.4203dup	NP_066399.2:p.Pro1403AlafsTer?