Canonical Allele Identifier: CA394303043

Gene: TSC2

Linked Data

• MyVariant Identifiers: chr16:g.2135017T>G (hg19) ; chr16:g.2085016T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2085016T>G , CM000678.2:g.2085016T>G	GRCh38
NC_000016.9:g.2135017T>G , CM000678.1:g.2135017T>G	GRCh37
NC_000016.8:g.2075018T>G	NCBI36
NG_005895.1:g.40711T>G , LRG_487:g.40711T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*2908T>G	ENSP00000455997.2:n.*2908T>G
ENST00000642206.2:c.4406T>G	ENSP00000495146.2:p.Leu1469Arg
ENST00000642365.2:c.4556T>G	ENSP00000495459.2:p.Leu1519Arg
ENST00000644417.2:c.*4939T>G	ENSP00000493912.2:n.*4939T>G
ENST00000646464.2:c.*7308T>G	ENSP00000496610.2:n.*7308T>G
ENST00000219476.9:c.4559T>G MANE Select	ENSP00000219476.3:p.Leu1520Arg
ENST00000350773.9:c.4490T>G	ENSP00000344383.4:p.Leu1497Arg
ENST00000401874.7:c.4358T>G	ENSP00000384468.2:p.Leu1453Arg
ENST00000568454.6:c.4391T>G	ENSP00000454487.1:p.Leu1464Arg
ENST00000569110.2:c.782T>G
ENST00000569930.2:n.2441T>G
ENST00000642365.1:c.3213T>G
ENST00000642561.1:c.4430T>G	ENSP00000495099.1:p.Leu1477Arg
ENST00000642728.1:n.741T>G
ENST00000642797.1:c.4361T>G	ENSP00000493846.1:p.Leu1454Arg
ENST00000642936.1:c.4427T>G	ENSP00000494514.1:p.Leu1476Arg
ENST00000643088.1:c.4358T>G	ENSP00000494747.1:p.Leu1453Arg
ENST00000643177.1:n.573T>G
ENST00000643426.1:n.2207T>G
ENST00000643946.1:c.4490T>G	ENSP00000495927.1:p.Leu1497Arg
ENST00000644043.1:c.4430T>G	ENSP00000496262.1:p.Leu1477Arg
ENST00000644329.1:c.4358T>G	ENSP00000496611.1:p.Leu1453Arg
ENST00000644335.1:c.4361T>G	ENSP00000496317.1:p.Leu1454Arg
ENST00000644399.1:c.4480T>G
ENST00000645024.1:n.2643T>G
ENST00000646388.1:c.4559T>G	ENSP00000495921.1:p.Leu1520Arg
ENST00000646634.1:n.3374T>G
ENST00000646674.1:n.1811T>G
ENST00000647042.1:n.1782T>G
ENST00000647180.1:n.1672T>G
ENST00000219476.7:c.4559T>G	ENSP00000219476.3:p.Leu1520Arg
ENST00000350773.8:c.4490T>G	ENSP00000344383.4:p.Leu1497Arg
ENST00000382538.10:c.4214T>G	ENSP00000371978.6:p.Leu1405Arg
ENST00000401874.6:c.4358T>G	ENSP00000384468.2:p.Leu1453Arg
ENST00000439117.6:c.*3726T>G	ENSP00000406980.2:n.*3726T>G
ENST00000439673.6:c.4250T>G	ENSP00000399232.2:p.Leu1417Arg
ENST00000497886.5:n.2317T>G
ENST00000568454.5:c.4391T>G	ENSP00000454487.1:p.Leu1464Arg
ENST00000569110.1:c.741T>G
ENST00000569930.1:n.1674T>G
NM_000548.3:c.4559T>G , LRG_487t1:c.4559T>G	NP_000539.2:p.Leu1520Arg
NM_001077183.1:c.4358T>G	NP_001070651.1:p.Leu1453Arg
NM_001114382.1:c.4490T>G	NP_001107854.1:p.Leu1497Arg
XM_005255529.3:c.4430T>G	XP_005255586.2:p.Leu1477Arg
XM_005255531.3:c.4361T>G	XP_005255588.2:p.Leu1454Arg
XM_011522636.1:c.4613T>G	XP_011520938.1:p.Leu1538Arg
XM_011522637.1:c.4610T>G	XP_011520939.1:p.Leu1537Arg
XM_011522638.1:c.4502T>G	XP_011520940.1:p.Leu1501Arg
XM_011522639.1:c.4484T>G	XP_011520941.1:p.Leu1495Arg
XM_011522640.1:c.4481T>G	XP_011520942.1:p.Leu1494Arg
XM_011522641.1:c.4250T>G	XP_011520943.1:p.Leu1417Arg
NM_000548.4:c.4559T>G	NP_000539.2:p.Leu1520Arg
NM_001077183.2:c.4358T>G	NP_001070651.1:p.Leu1453Arg
NM_001114382.2:c.4490T>G	NP_001107854.1:p.Leu1497Arg
NM_001318827.1:c.4250T>G	NP_001305756.1:p.Leu1417Arg
NM_001318829.1:c.4214T>G	NP_001305758.1:p.Leu1405Arg
NM_001318831.1:c.3827T>G	NP_001305760.1:p.Leu1276Arg
NM_001318832.1:c.4391T>G	NP_001305761.1:p.Leu1464Arg
NM_001363528.1:c.4361T>G	NP_001350457.1:p.Leu1454Arg
NM_021055.2:c.4430T>G	NP_066399.2:p.Leu1477Arg
XM_005255531.4:c.4361T>G	XP_005255588.2:p.Leu1454Arg
XM_011522636.2:c.4613T>G	XP_011520938.1:p.Leu1538Arg
XM_011522637.2:c.4610T>G	XP_011520939.1:p.Leu1537Arg
XM_011522638.2:c.4775T>G	XP_011520940.2:p.Leu1592Arg
XM_011522639.2:c.4484T>G	XP_011520941.1:p.Leu1495Arg
XM_011522640.2:c.4481T>G	XP_011520942.1:p.Leu1494Arg
XM_017023615.1:c.4556T>G	XP_016879104.1:p.Leu1519Arg
XM_017023616.1:c.4427T>G	XP_016879105.1:p.Leu1476Arg
XM_017023617.1:c.4523T>G	XP_016879106.1:p.Leu1508Arg
XM_017023618.1:c.3269T>G	XP_016879107.1:p.Leu1090Arg
XM_024450413.1:c.4358T>G	XP_024306181.1:p.Leu1453Arg
NM_000548.5:c.4559T>G MANE Select	NP_000539.2:p.Leu1520Arg
NM_001370404.1:c.4427T>G	NP_001357333.1:p.Leu1476Arg
NM_001370405.1:c.4430T>G	NP_001357334.1:p.Leu1477Arg
NM_001077183.3:c.4358T>G	NP_001070651.1:p.Leu1453Arg
NM_001114382.3:c.4490T>G	NP_001107854.1:p.Leu1497Arg
NM_001318827.2:c.4250T>G	NP_001305756.1:p.Leu1417Arg
NM_001318829.2:c.4214T>G	NP_001305758.1:p.Leu1405Arg
NM_001318831.2:c.3827T>G	NP_001305760.1:p.Leu1276Arg
NM_001318832.2:c.4391T>G	NP_001305761.1:p.Leu1464Arg
NM_001363528.2:c.4361T>G	NP_001350457.1:p.Leu1454Arg
NM_021055.3:c.4430T>G	NP_066399.2:p.Leu1477Arg