Canonical Allele Identifier: CA2202019086

Gene: TSC2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2085236T= , CM000678.2:g.2085236T=	GRCh38
NC_000016.9:g.2135237T= , CM000678.1:g.2135237T=	GRCh37
NC_000016.8:g.2075238T=	NCBI36
NG_005895.1:g.40931T= , LRG_487:g.40931T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*2925T=	ENSP00000455997.2:n.*2925T=
ENST00000642206.2:c.4423T=	ENSP00000495146.2:p.Ser1475=
ENST00000642365.2:c.4573T=	ENSP00000495459.2:p.Ser1525=
ENST00000644417.2:c.*4956T=	ENSP00000493912.2:n.*4956T=
ENST00000646464.2:c.*7325T=	ENSP00000496610.2:n.*7325T=
ENST00000219476.9:c.4576T= MANE Select	ENSP00000219476.3:p.Ser1526=
ENST00000350773.9:c.4507T=	ENSP00000344383.4:p.Ser1503=
ENST00000401874.7:c.4375T=	ENSP00000384468.2:p.Ser1459=
ENST00000568454.6:c.4408T=	ENSP00000454487.1:p.Ser1470=
ENST00000569110.2:c.799T=
ENST00000569930.2:n.2458T=
ENST00000642365.1:c.3230T=
ENST00000642561.1:c.4447T=	ENSP00000495099.1:p.Ser1483=
ENST00000642728.1:n.758T=
ENST00000642791.1:n.173T=
ENST00000642797.1:c.4378T=	ENSP00000493846.1:p.Ser1460=
ENST00000642936.1:c.4444T=	ENSP00000494514.1:p.Ser1482=
ENST00000643088.1:c.4369T=	ENSP00000494747.1:p.Ser1457=
ENST00000643177.1:n.590T=
ENST00000643426.1:n.2224T=
ENST00000643946.1:c.4501T=	ENSP00000495927.1:p.Ser1501=
ENST00000644043.1:c.4447T=	ENSP00000496262.1:p.Ser1483=
ENST00000644278.1:n.58T=
ENST00000644329.1:c.4375T=	ENSP00000496611.1:p.Ser1459=
ENST00000644335.1:c.4372T=	ENSP00000496317.1:p.Ser1458=
ENST00000644399.1:c.4497T=
ENST00000645024.1:n.2660T=
ENST00000646388.1:c.4570T=	ENSP00000495921.1:p.Ser1524=
ENST00000646634.1:n.3391T=
ENST00000646674.1:n.1828T=
ENST00000647042.1:n.1799T=
ENST00000647180.1:n.1689T=
ENST00000219476.7:c.4576T=	ENSP00000219476.3:p.Ser1526=
ENST00000350773.8:c.4507T=	ENSP00000344383.4:p.Ser1503=
ENST00000382538.10:c.4231T=	ENSP00000371978.6:p.Ser1411=
ENST00000401874.6:c.4375T=	ENSP00000384468.2:p.Ser1459=
ENST00000439117.6:c.*3743T=	ENSP00000406980.2:n.*3743T=
ENST00000439673.6:c.4267T=	ENSP00000399232.2:p.Ser1423=
ENST00000497886.5:n.2334T=
ENST00000568454.5:c.4408T=	ENSP00000454487.1:p.Ser1470=
ENST00000569110.1:c.758T=
ENST00000569930.1:n.1691T=
NM_000548.3:c.4576T= , LRG_487t1:c.4576T=	NP_000539.2:p.Ser1526=
NM_001077183.1:c.4375T=	NP_001070651.1:p.Ser1459=
NM_001114382.1:c.4507T=	NP_001107854.1:p.Ser1503=
XM_005255529.3:c.4447T=	XP_005255586.2:p.Ser1483=
XM_005255531.3:c.4378T=	XP_005255588.2:p.Ser1460=
XM_011522636.1:c.4630T=	XP_011520938.1:p.Ser1544=
XM_011522637.1:c.4627T=	XP_011520939.1:p.Ser1543=
XM_011522638.1:c.4519T=	XP_011520940.1:p.Ser1507=
XM_011522639.1:c.4501T=	XP_011520941.1:p.Ser1501=
XM_011522640.1:c.4498T=	XP_011520942.1:p.Ser1500=
XM_011522641.1:c.4267T=	XP_011520943.1:p.Ser1423=
NM_000548.4:c.4576T=	NP_000539.2:p.Ser1526=
NM_001077183.2:c.4375T=	NP_001070651.1:p.Ser1459=
NM_001114382.2:c.4507T=	NP_001107854.1:p.Ser1503=
NM_001318827.1:c.4267T=	NP_001305756.1:p.Ser1423=
NM_001318829.1:c.4231T=	NP_001305758.1:p.Ser1411=
NM_001318831.1:c.3844T=	NP_001305760.1:p.Ser1282=
NM_001318832.1:c.4408T=	NP_001305761.1:p.Ser1470=
NM_001363528.1:c.4378T=	NP_001350457.1:p.Ser1460=
NM_021055.2:c.4447T=	NP_066399.2:p.Ser1483=
XM_005255531.4:c.4378T=	XP_005255588.2:p.Ser1460=
XM_011522636.2:c.4630T=	XP_011520938.1:p.Ser1544=
XM_011522637.2:c.4627T=	XP_011520939.1:p.Ser1543=
XM_011522638.2:c.4792T=	XP_011520940.2:p.Ser1598=
XM_011522639.2:c.4501T=	XP_011520941.1:p.Ser1501=
XM_011522640.2:c.4498T=	XP_011520942.1:p.Ser1500=
XM_017023615.1:c.4573T=	XP_016879104.1:p.Ser1525=
XM_017023616.1:c.4444T=	XP_016879105.1:p.Ser1482=
XM_017023617.1:c.4540T=	XP_016879106.1:p.Ser1514=
XM_017023618.1:c.3286T=	XP_016879107.1:p.Ser1096=
XM_024450413.1:c.4375T=	XP_024306181.1:p.Ser1459=
NM_000548.5:c.4576T= MANE Select	NP_000539.2:p.Ser1526=
NM_001370404.1:c.4444T=	NP_001357333.1:p.Ser1482=
NM_001370405.1:c.4447T=	NP_001357334.1:p.Ser1483=
NM_001077183.3:c.4375T=	NP_001070651.1:p.Ser1459=
NM_001114382.3:c.4507T=	NP_001107854.1:p.Ser1503=
NM_001318827.2:c.4267T=	NP_001305756.1:p.Ser1423=
NM_001318829.2:c.4231T=	NP_001305758.1:p.Ser1411=
NM_001318831.2:c.3844T=	NP_001305760.1:p.Ser1282=
NM_001318832.2:c.4408T=	NP_001305761.1:p.Ser1470=
NM_001363528.2:c.4378T=	NP_001350457.1:p.Ser1460=
NM_021055.3:c.4447T=	NP_066399.2:p.Ser1483=