Canonical Allele Identifier: CA2202018183
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2084992A= , CM000678.2:g.2084992A= GRCh38
NC_000016.9:g.2134993A= , CM000678.1:g.2134993A= GRCh37
NC_000016.8:g.2074994A= NCBI36
NG_005895.1:g.40687A= , LRG_487:g.40687A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*2884A= ENSP00000455997.2:n.*2884A=
ENST00000642206.2:c.4382A= ENSP00000495146.2:p.Asp1461=
ENST00000642365.2:c.4532A= ENSP00000495459.2:p.Asp1511=
ENST00000644417.2:c.*4915A= ENSP00000493912.2:n.*4915A=
ENST00000646464.2:c.*7284A= ENSP00000496610.2:n.*7284A=
ENST00000219476.9:c.4535A= MANE Select ENSP00000219476.3:p.Asp1512=
ENST00000350773.9:c.4466A= ENSP00000344383.4:p.Asp1489=
ENST00000401874.7:c.4334A= ENSP00000384468.2:p.Asp1445=
ENST00000568454.6:c.4367A= ENSP00000454487.1:p.Asp1456=
ENST00000569110.2:c.758A=
ENST00000569930.2:n.2417A=
ENST00000642365.1:c.3189A=
ENST00000642561.1:c.4406A= ENSP00000495099.1:p.Asp1469=
ENST00000642728.1:n.717A=
ENST00000642797.1:c.4337A= ENSP00000493846.1:p.Asp1446=
ENST00000642936.1:c.4403A= ENSP00000494514.1:p.Asp1468=
ENST00000643088.1:c.4334A= ENSP00000494747.1:p.Asp1445=
ENST00000643177.1:n.549A=
ENST00000643426.1:n.2183A=
ENST00000643946.1:c.4466A= ENSP00000495927.1:p.Asp1489=
ENST00000644043.1:c.4406A= ENSP00000496262.1:p.Asp1469=
ENST00000644329.1:c.4334A= ENSP00000496611.1:p.Asp1445=
ENST00000644335.1:c.4337A= ENSP00000496317.1:p.Asp1446=
ENST00000644399.1:c.4456A=
ENST00000645024.1:n.2619A=
ENST00000646388.1:c.4535A= ENSP00000495921.1:p.Asp1512=
ENST00000646634.1:n.3350A=
ENST00000646674.1:n.1787A=
ENST00000647042.1:n.1758A=
ENST00000647180.1:n.1648A=
ENST00000219476.7:c.4535A= ENSP00000219476.3:p.Asp1512=
ENST00000350773.8:c.4466A= ENSP00000344383.4:p.Asp1489=
ENST00000382538.10:c.4190A= ENSP00000371978.6:p.Asp1397=
ENST00000401874.6:c.4334A= ENSP00000384468.2:p.Asp1445=
ENST00000439117.6:c.*3702A= ENSP00000406980.2:n.*3702A=
ENST00000439673.6:c.4226A= ENSP00000399232.2:p.Asp1409=
ENST00000497886.5:n.2293A=
ENST00000568454.5:c.4367A= ENSP00000454487.1:p.Asp1456=
ENST00000569110.1:c.717A=
ENST00000569930.1:n.1650A=
NM_000548.3:c.4535A= , LRG_487t1:c.4535A= NP_000539.2:p.Asp1512=
NM_001077183.1:c.4334A= NP_001070651.1:p.Asp1445=
NM_001114382.1:c.4466A= NP_001107854.1:p.Asp1489=
XM_005255529.3:c.4406A= XP_005255586.2:p.Asp1469=
XM_005255531.3:c.4337A= XP_005255588.2:p.Asp1446=
XM_011522636.1:c.4589A= XP_011520938.1:p.Asp1530=
XM_011522637.1:c.4586A= XP_011520939.1:p.Asp1529=
XM_011522638.1:c.4478A= XP_011520940.1:p.Asp1493=
XM_011522639.1:c.4460A= XP_011520941.1:p.Asp1487=
XM_011522640.1:c.4457A= XP_011520942.1:p.Asp1486=
XM_011522641.1:c.4226A= XP_011520943.1:p.Asp1409=
NM_000548.4:c.4535A= NP_000539.2:p.Asp1512=
NM_001077183.2:c.4334A= NP_001070651.1:p.Asp1445=
NM_001114382.2:c.4466A= NP_001107854.1:p.Asp1489=
NM_001318827.1:c.4226A= NP_001305756.1:p.Asp1409=
NM_001318829.1:c.4190A= NP_001305758.1:p.Asp1397=
NM_001318831.1:c.3803A= NP_001305760.1:p.Asp1268=
NM_001318832.1:c.4367A= NP_001305761.1:p.Asp1456=
NM_001363528.1:c.4337A= NP_001350457.1:p.Asp1446=
NM_021055.2:c.4406A= NP_066399.2:p.Asp1469=
XM_005255531.4:c.4337A= XP_005255588.2:p.Asp1446=
XM_011522636.2:c.4589A= XP_011520938.1:p.Asp1530=
XM_011522637.2:c.4586A= XP_011520939.1:p.Asp1529=
XM_011522638.2:c.4751A= XP_011520940.2:p.Asp1584=
XM_011522639.2:c.4460A= XP_011520941.1:p.Asp1487=
XM_011522640.2:c.4457A= XP_011520942.1:p.Asp1486=
XM_017023615.1:c.4532A= XP_016879104.1:p.Asp1511=
XM_017023616.1:c.4403A= XP_016879105.1:p.Asp1468=
XM_017023617.1:c.4499A= XP_016879106.1:p.Asp1500=
XM_017023618.1:c.3245A= XP_016879107.1:p.Asp1082=
XM_024450413.1:c.4334A= XP_024306181.1:p.Asp1445=
NM_000548.5:c.4535A= MANE Select NP_000539.2:p.Asp1512=
NM_001370404.1:c.4403A= NP_001357333.1:p.Asp1468=
NM_001370405.1:c.4406A= NP_001357334.1:p.Asp1469=
NM_001077183.3:c.4334A= NP_001070651.1:p.Asp1445=
NM_001114382.3:c.4466A= NP_001107854.1:p.Asp1489=
NM_001318827.2:c.4226A= NP_001305756.1:p.Asp1409=
NM_001318829.2:c.4190A= NP_001305758.1:p.Asp1397=
NM_001318831.2:c.3803A= NP_001305760.1:p.Asp1268=
NM_001318832.2:c.4367A= NP_001305761.1:p.Asp1456=
NM_001363528.2:c.4337A= NP_001350457.1:p.Asp1446=
NM_021055.3:c.4406A= NP_066399.2:p.Asp1469=