Canonical Allele Identifier: CA2202028982

Gene: TSC2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2079347_2079349delinsCTG , CM000678.2:g.2079347_2079349delinsCTG	GRCh38
NC_000016.9:g.2129348_2129350delinsCTG , CM000678.1:g.2129348_2129350delinsCTG	GRCh37
NC_000016.8:g.2069349_2069351delinsCTG	NCBI36
NG_005895.1:g.35042_35044delinsCTG , LRG_487:g.35042_35044delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*1621_*1623delinsCTG	ENSP00000455997.2:n.*1621_*1623delinsCTG
ENST00000642206.2:c.3119_3121delinsCTG	ENSP00000495146.2:p.Thr1040=
ENST00000642365.2:c.3200_3202delinsCTG	ENSP00000495459.2:p.Thr1067=
ENST00000644417.2:c.*3652_*3654delinsCTG	ENSP00000493912.2:n.*3652_*3654delinsCTG
ENST00000646464.2:c.*4125_*4127delinsCTG	ENSP00000496610.2:n.*4125_*4127delinsCTG
ENST00000219476.9:c.3203_3205delinsCTG MANE Select	ENSP00000219476.3:p.Thr1068=
ENST00000350773.9:c.3203_3205delinsCTG	ENSP00000344383.4:p.Thr1068=
ENST00000401874.7:c.3071_3073delinsCTG	ENSP00000384468.2:p.Thr1024=
ENST00000471143.6:c.431_433delinsCTG	ENSP00000458541.2:n.431_433delinsCTG
ENST00000568366.6:n.560_562delinsCTG
ENST00000568454.6:c.3104_3106delinsCTG	ENSP00000454487.1:p.Thr1035=
ENST00000642365.1:c.1857_1859delinsCTG
ENST00000642561.1:c.3074_3076delinsCTG	ENSP00000495099.1:p.Thr1025=
ENST00000642797.1:c.3074_3076delinsCTG	ENSP00000493846.1:p.Thr1025=
ENST00000642936.1:c.3071_3073delinsCTG	ENSP00000494514.1:p.Thr1024=
ENST00000643088.1:c.3071_3073delinsCTG	ENSP00000494747.1:p.Thr1024=
ENST00000643946.1:c.3203_3205delinsCTG	ENSP00000495927.1:p.Thr1068=
ENST00000644043.1:c.3074_3076delinsCTG	ENSP00000496262.1:p.Thr1025=
ENST00000644329.1:c.3071_3073delinsCTG	ENSP00000496611.1:p.Thr1024=
ENST00000644335.1:c.3074_3076delinsCTG	ENSP00000496317.1:p.Thr1025=
ENST00000644399.1:c.3193_3195delinsCTG
ENST00000644722.1:n.349_351delinsCTG
ENST00000645024.1:n.1356_1358delinsCTG
ENST00000646388.1:c.3203_3205delinsCTG	ENSP00000495921.1:p.Thr1068=
ENST00000646634.1:n.2087_2089delinsCTG
ENST00000647042.1:n.495_497delinsCTG
ENST00000219476.7:c.3203_3205delinsCTG	ENSP00000219476.3:p.Thr1068=
ENST00000350773.8:c.3203_3205delinsCTG	ENSP00000344383.4:p.Thr1068=
ENST00000382538.10:c.2927_2929delinsCTG	ENSP00000371978.6:p.Thr976=
ENST00000401874.6:c.3071_3073delinsCTG	ENSP00000384468.2:p.Thr1024=
ENST00000439117.6:c.*2370_*2372delinsCTG	ENSP00000406980.2:n.*2370_*2372delinsCTG
ENST00000439673.6:c.2963_2965delinsCTG	ENSP00000399232.2:p.Thr988=
ENST00000471143.5:c.429_431delinsCTG
ENST00000483020.5:c.443_445delinsCTG	ENSP00000460310.1:n.443_445delinsCTG
ENST00000497886.5:n.1030_1032delinsCTG
ENST00000561695.1:n.428_430delinsCTG
ENST00000568366.5:n.560_562delinsCTG
ENST00000568454.5:c.3104_3106delinsCTG	ENSP00000454487.1:p.Thr1035=
NM_000548.3:c.3203_3205delinsCTG , LRG_487t1:c.3203_3205delinsCTG	NP_000539.2:p.Thr1068=
NM_001077183.1:c.3071_3073delinsCTG	NP_001070651.1:p.Thr1024=
NM_001114382.1:c.3203_3205delinsCTG	NP_001107854.1:p.Thr1068=
XM_005255529.3:c.3074_3076delinsCTG	XP_005255586.2:p.Thr1025=
XM_005255531.3:c.3074_3076delinsCTG	XP_005255588.2:p.Thr1025=
XM_011522636.1:c.3203_3205delinsCTG	XP_011520938.1:p.Thr1068=
XM_011522637.1:c.3200_3202delinsCTG	XP_011520939.1:p.Thr1067=
XM_011522638.1:c.3092_3094delinsCTG	XP_011520940.1:p.Thr1031=
XM_011522639.1:c.3074_3076delinsCTG	XP_011520941.1:p.Thr1025=
XM_011522640.1:c.3071_3073delinsCTG	XP_011520942.1:p.Thr1024=
XM_011522641.1:c.2963_2965delinsCTG	XP_011520943.1:p.Thr988=
NM_000548.4:c.3203_3205delinsCTG	NP_000539.2:p.Thr1068=
NM_001077183.2:c.3071_3073delinsCTG	NP_001070651.1:p.Thr1024=
NM_001114382.2:c.3203_3205delinsCTG	NP_001107854.1:p.Thr1068=
NM_001318827.1:c.2963_2965delinsCTG	NP_001305756.1:p.Thr988=
NM_001318829.1:c.2927_2929delinsCTG	NP_001305758.1:p.Thr976=
NM_001318831.1:c.2471_2473delinsCTG	NP_001305760.1:p.Thr824=
NM_001318832.1:c.3104_3106delinsCTG	NP_001305761.1:p.Thr1035=
NM_001363528.1:c.3074_3076delinsCTG	NP_001350457.1:p.Thr1025=
NM_021055.2:c.3074_3076delinsCTG	NP_066399.2:p.Thr1025=
XM_005255531.4:c.3074_3076delinsCTG	XP_005255588.2:p.Thr1025=
XM_011522636.2:c.3203_3205delinsCTG	XP_011520938.1:p.Thr1068=
XM_011522637.2:c.3200_3202delinsCTG	XP_011520939.1:p.Thr1067=
XM_011522638.2:c.3365_3367delinsCTG	XP_011520940.2:p.Thr1122=
XM_011522639.2:c.3074_3076delinsCTG	XP_011520941.1:p.Thr1025=
XM_011522640.2:c.3071_3073delinsCTG	XP_011520942.1:p.Thr1024=
XM_017023615.1:c.3200_3202delinsCTG	XP_016879104.1:p.Thr1067=
XM_017023616.1:c.3071_3073delinsCTG	XP_016879105.1:p.Thr1024=
XM_017023617.1:c.3236_3238delinsCTG	XP_016879106.1:p.Thr1079=
XM_017023618.1:c.1859_1861delinsCTG	XP_016879107.1:p.Thr620=
XM_024450413.1:c.3071_3073delinsCTG	XP_024306181.1:p.Thr1024=
NM_000548.5:c.3203_3205delinsCTG MANE Select	NP_000539.2:p.Thr1068=
NM_001370404.1:c.3071_3073delinsCTG	NP_001357333.1:p.Thr1024=
NM_001370405.1:c.3074_3076delinsCTG	NP_001357334.1:p.Thr1025=
NM_001077183.3:c.3071_3073delinsCTG	NP_001070651.1:p.Thr1024=
NM_001114382.3:c.3203_3205delinsCTG	NP_001107854.1:p.Thr1068=
NM_001318827.2:c.2963_2965delinsCTG	NP_001305756.1:p.Thr988=
NM_001318829.2:c.2927_2929delinsCTG	NP_001305758.1:p.Thr976=
NM_001318831.2:c.2471_2473delinsCTG	NP_001305760.1:p.Thr824=
NM_001318832.2:c.3104_3106delinsCTG	NP_001305761.1:p.Thr1035=
NM_001363528.2:c.3074_3076delinsCTG	NP_001350457.1:p.Thr1025=
NM_021055.3:c.3074_3076delinsCTG	NP_066399.2:p.Thr1025=