Canonical Allele Identifier: CA394304402

Gene: TSC2

Linked Data

• ClinVar Variation Id: 2705118
• ClinVar RCV Id: RCV003512908
• MyVariant Identifiers: chr16:g.2135242T>G (hg19) ; chr16:g.2085241T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2085241T>G , CM000678.2:g.2085241T>G	GRCh38
NC_000016.9:g.2135242T>G , CM000678.1:g.2135242T>G	GRCh37
NC_000016.8:g.2075243T>G	NCBI36
NG_005895.1:g.40936T>G , LRG_487:g.40936T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*2930T>G	ENSP00000455997.2:n.*2930T>G
ENST00000642206.2:c.4428T>G	ENSP00000495146.2:p.Phe1476Leu
ENST00000642365.2:c.4578T>G	ENSP00000495459.2:p.Phe1526Leu
ENST00000644417.2:c.*4961T>G	ENSP00000493912.2:n.*4961T>G
ENST00000646464.2:c.*7330T>G	ENSP00000496610.2:n.*7330T>G
ENST00000219476.9:c.4581T>G MANE Select	ENSP00000219476.3:p.Phe1527Leu
ENST00000350773.9:c.4512T>G	ENSP00000344383.4:p.Phe1504Leu
ENST00000401874.7:c.4380T>G	ENSP00000384468.2:p.Phe1460Leu
ENST00000568454.6:c.4413T>G	ENSP00000454487.1:p.Phe1471Leu
ENST00000569110.2:c.804T>G
ENST00000569930.2:n.2463T>G
ENST00000642365.1:c.3235T>G
ENST00000642561.1:c.4452T>G	ENSP00000495099.1:p.Phe1484Leu
ENST00000642728.1:n.763T>G
ENST00000642791.1:n.178T>G
ENST00000642797.1:c.4383T>G	ENSP00000493846.1:p.Phe1461Leu
ENST00000642936.1:c.4449T>G	ENSP00000494514.1:p.Phe1483Leu
ENST00000643088.1:c.4374T>G	ENSP00000494747.1:p.Phe1458Leu
ENST00000643177.1:n.595T>G
ENST00000643426.1:n.2229T>G
ENST00000643946.1:c.4506T>G	ENSP00000495927.1:p.Phe1502Leu
ENST00000644043.1:c.4452T>G	ENSP00000496262.1:p.Phe1484Leu
ENST00000644278.1:n.63T>G
ENST00000644329.1:c.4380T>G	ENSP00000496611.1:p.Phe1460Leu
ENST00000644335.1:c.4377T>G	ENSP00000496317.1:p.Phe1459Leu
ENST00000644399.1:c.4502T>G
ENST00000645024.1:n.2665T>G
ENST00000646388.1:c.4575T>G	ENSP00000495921.1:p.Phe1525Leu
ENST00000646634.1:n.3396T>G
ENST00000646674.1:n.1833T>G
ENST00000647042.1:n.1804T>G
ENST00000647180.1:n.1694T>G
ENST00000219476.7:c.4581T>G	ENSP00000219476.3:p.Phe1527Leu
ENST00000350773.8:c.4512T>G	ENSP00000344383.4:p.Phe1504Leu
ENST00000382538.10:c.4236T>G	ENSP00000371978.6:p.Phe1412Leu
ENST00000401874.6:c.4380T>G	ENSP00000384468.2:p.Phe1460Leu
ENST00000439117.6:c.*3748T>G	ENSP00000406980.2:n.*3748T>G
ENST00000439673.6:c.4272T>G	ENSP00000399232.2:p.Phe1424Leu
ENST00000497886.5:n.2339T>G
ENST00000568454.5:c.4413T>G	ENSP00000454487.1:p.Phe1471Leu
ENST00000569110.1:c.763T>G
ENST00000569930.1:n.1696T>G
NM_000548.3:c.4581T>G , LRG_487t1:c.4581T>G	NP_000539.2:p.Phe1527Leu
NM_001077183.1:c.4380T>G	NP_001070651.1:p.Phe1460Leu
NM_001114382.1:c.4512T>G	NP_001107854.1:p.Phe1504Leu
XM_005255529.3:c.4452T>G	XP_005255586.2:p.Phe1484Leu
XM_005255531.3:c.4383T>G	XP_005255588.2:p.Phe1461Leu
XM_011522636.1:c.4635T>G	XP_011520938.1:p.Phe1545Leu
XM_011522637.1:c.4632T>G	XP_011520939.1:p.Phe1544Leu
XM_011522638.1:c.4524T>G	XP_011520940.1:p.Phe1508Leu
XM_011522639.1:c.4506T>G	XP_011520941.1:p.Phe1502Leu
XM_011522640.1:c.4503T>G	XP_011520942.1:p.Phe1501Leu
XM_011522641.1:c.4272T>G	XP_011520943.1:p.Phe1424Leu
NM_000548.4:c.4581T>G	NP_000539.2:p.Phe1527Leu
NM_001077183.2:c.4380T>G	NP_001070651.1:p.Phe1460Leu
NM_001114382.2:c.4512T>G	NP_001107854.1:p.Phe1504Leu
NM_001318827.1:c.4272T>G	NP_001305756.1:p.Phe1424Leu
NM_001318829.1:c.4236T>G	NP_001305758.1:p.Phe1412Leu
NM_001318831.1:c.3849T>G	NP_001305760.1:p.Phe1283Leu
NM_001318832.1:c.4413T>G	NP_001305761.1:p.Phe1471Leu
NM_001363528.1:c.4383T>G	NP_001350457.1:p.Phe1461Leu
NM_021055.2:c.4452T>G	NP_066399.2:p.Phe1484Leu
XM_005255531.4:c.4383T>G	XP_005255588.2:p.Phe1461Leu
XM_011522636.2:c.4635T>G	XP_011520938.1:p.Phe1545Leu
XM_011522637.2:c.4632T>G	XP_011520939.1:p.Phe1544Leu
XM_011522638.2:c.4797T>G	XP_011520940.2:p.Phe1599Leu
XM_011522639.2:c.4506T>G	XP_011520941.1:p.Phe1502Leu
XM_011522640.2:c.4503T>G	XP_011520942.1:p.Phe1501Leu
XM_017023615.1:c.4578T>G	XP_016879104.1:p.Phe1526Leu
XM_017023616.1:c.4449T>G	XP_016879105.1:p.Phe1483Leu
XM_017023617.1:c.4545T>G	XP_016879106.1:p.Phe1515Leu
XM_017023618.1:c.3291T>G	XP_016879107.1:p.Phe1097Leu
XM_024450413.1:c.4380T>G	XP_024306181.1:p.Phe1460Leu
NM_000548.5:c.4581T>G MANE Select	NP_000539.2:p.Phe1527Leu
NM_001370404.1:c.4449T>G	NP_001357333.1:p.Phe1483Leu
NM_001370405.1:c.4452T>G	NP_001357334.1:p.Phe1484Leu
NM_001077183.3:c.4380T>G	NP_001070651.1:p.Phe1460Leu
NM_001114382.3:c.4512T>G	NP_001107854.1:p.Phe1504Leu
NM_001318827.2:c.4272T>G	NP_001305756.1:p.Phe1424Leu
NM_001318829.2:c.4236T>G	NP_001305758.1:p.Phe1412Leu
NM_001318831.2:c.3849T>G	NP_001305760.1:p.Phe1283Leu
NM_001318832.2:c.4413T>G	NP_001305761.1:p.Phe1471Leu
NM_001363528.2:c.4383T>G	NP_001350457.1:p.Phe1461Leu
NM_021055.3:c.4452T>G	NP_066399.2:p.Phe1484Leu