Canonical Allele Identifier: CA394305070

Gene: TSC2

Linked Data

• dbSNP Id: rs878854110
• MyVariant Identifiers: chr16:g.2135317A>T (hg19) ; chr16:g.2085316A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2085316A>T , CM000678.2:g.2085316A>T	GRCh38
NC_000016.9:g.2135317A>T , CM000678.1:g.2135317A>T	GRCh37
NC_000016.8:g.2075318A>T	NCBI36
NG_005895.1:g.41011A>T , LRG_487:g.41011A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*3005A>T	ENSP00000455997.2:n.*3005A>T
ENST00000642206.2:c.4503A>T	ENSP00000495146.2:p.Glu1501Asp
ENST00000642365.2:c.4653A>T	ENSP00000495459.2:p.Glu1551Asp
ENST00000644417.2:c.*5036A>T	ENSP00000493912.2:n.*5036A>T
ENST00000646464.2:c.*7405A>T	ENSP00000496610.2:n.*7405A>T
ENST00000219476.9:c.4656A>T MANE Select	ENSP00000219476.3:p.Glu1552Asp
ENST00000350773.9:c.4587A>T	ENSP00000344383.4:p.Glu1529Asp
ENST00000401874.7:c.4455A>T	ENSP00000384468.2:p.Glu1485Asp
ENST00000568454.6:c.4488A>T	ENSP00000454487.1:p.Glu1496Asp
ENST00000569110.2:c.879A>T
ENST00000569930.2:n.2538A>T
ENST00000642365.1:c.3310A>T
ENST00000642561.1:c.4527A>T	ENSP00000495099.1:p.Glu1509Asp
ENST00000642728.1:n.838A>T
ENST00000642791.1:n.253A>T
ENST00000642797.1:c.4458A>T	ENSP00000493846.1:p.Glu1486Asp
ENST00000642936.1:c.4524A>T	ENSP00000494514.1:p.Glu1508Asp
ENST00000643088.1:c.4449A>T	ENSP00000494747.1:p.Glu1483Asp
ENST00000643177.1:n.670A>T
ENST00000643426.1:n.2304A>T
ENST00000643946.1:c.4581A>T	ENSP00000495927.1:p.Glu1527Asp
ENST00000644043.1:c.4527A>T	ENSP00000496262.1:p.Glu1509Asp
ENST00000644278.1:n.138A>T
ENST00000644329.1:c.4455A>T	ENSP00000496611.1:p.Glu1485Asp
ENST00000644335.1:c.4452A>T	ENSP00000496317.1:p.Glu1484Asp
ENST00000644399.1:c.4577A>T
ENST00000645024.1:n.2740A>T
ENST00000646388.1:c.4650A>T	ENSP00000495921.1:p.Glu1550Asp
ENST00000646634.1:n.3471A>T
ENST00000646674.1:n.1908A>T
ENST00000647042.1:n.1879A>T
ENST00000647180.1:n.1769A>T
ENST00000219476.7:c.4656A>T	ENSP00000219476.3:p.Glu1552Asp
ENST00000350773.8:c.4587A>T	ENSP00000344383.4:p.Glu1529Asp
ENST00000382538.10:c.4311A>T	ENSP00000371978.6:p.Glu1437Asp
ENST00000401874.6:c.4455A>T	ENSP00000384468.2:p.Glu1485Asp
ENST00000439117.6:c.*3823A>T	ENSP00000406980.2:n.*3823A>T
ENST00000439673.6:c.4347A>T	ENSP00000399232.2:p.Glu1449Asp
ENST00000497886.5:n.2414A>T
ENST00000568454.5:c.4488A>T	ENSP00000454487.1:p.Glu1496Asp
ENST00000569110.1:c.838A>T
ENST00000569930.1:n.1771A>T
NM_000548.3:c.4656A>T , LRG_487t1:c.4656A>T	NP_000539.2:p.Glu1552Asp
NM_001077183.1:c.4455A>T	NP_001070651.1:p.Glu1485Asp
NM_001114382.1:c.4587A>T	NP_001107854.1:p.Glu1529Asp
XM_005255529.3:c.4527A>T	XP_005255586.2:p.Glu1509Asp
XM_005255531.3:c.4458A>T	XP_005255588.2:p.Glu1486Asp
XM_011522636.1:c.4710A>T	XP_011520938.1:p.Glu1570Asp
XM_011522637.1:c.4707A>T	XP_011520939.1:p.Glu1569Asp
XM_011522638.1:c.4599A>T	XP_011520940.1:p.Glu1533Asp
XM_011522639.1:c.4581A>T	XP_011520941.1:p.Glu1527Asp
XM_011522640.1:c.4578A>T	XP_011520942.1:p.Glu1526Asp
XM_011522641.1:c.4347A>T	XP_011520943.1:p.Glu1449Asp
NM_000548.4:c.4656A>T	NP_000539.2:p.Glu1552Asp
NM_001077183.2:c.4455A>T	NP_001070651.1:p.Glu1485Asp
NM_001114382.2:c.4587A>T	NP_001107854.1:p.Glu1529Asp
NM_001318827.1:c.4347A>T	NP_001305756.1:p.Glu1449Asp
NM_001318829.1:c.4311A>T	NP_001305758.1:p.Glu1437Asp
NM_001318831.1:c.3924A>T	NP_001305760.1:p.Glu1308Asp
NM_001318832.1:c.4488A>T	NP_001305761.1:p.Glu1496Asp
NM_001363528.1:c.4458A>T	NP_001350457.1:p.Glu1486Asp
NM_021055.2:c.4527A>T	NP_066399.2:p.Glu1509Asp
XM_005255531.4:c.4458A>T	XP_005255588.2:p.Glu1486Asp
XM_011522636.2:c.4710A>T	XP_011520938.1:p.Glu1570Asp
XM_011522637.2:c.4707A>T	XP_011520939.1:p.Glu1569Asp
XM_011522638.2:c.4872A>T	XP_011520940.2:p.Glu1624Asp
XM_011522639.2:c.4581A>T	XP_011520941.1:p.Glu1527Asp
XM_011522640.2:c.4578A>T	XP_011520942.1:p.Glu1526Asp
XM_017023615.1:c.4653A>T	XP_016879104.1:p.Glu1551Asp
XM_017023616.1:c.4524A>T	XP_016879105.1:p.Glu1508Asp
XM_017023617.1:c.4620A>T	XP_016879106.1:p.Glu1540Asp
XM_017023618.1:c.3366A>T	XP_016879107.1:p.Glu1122Asp
XM_024450413.1:c.4455A>T	XP_024306181.1:p.Glu1485Asp
NM_000548.5:c.4656A>T MANE Select	NP_000539.2:p.Glu1552Asp
NM_001370404.1:c.4524A>T	NP_001357333.1:p.Glu1508Asp
NM_001370405.1:c.4527A>T	NP_001357334.1:p.Glu1509Asp
NM_001077183.3:c.4455A>T	NP_001070651.1:p.Glu1485Asp
NM_001114382.3:c.4587A>T	NP_001107854.1:p.Glu1529Asp
NM_001318827.2:c.4347A>T	NP_001305756.1:p.Glu1449Asp
NM_001318829.2:c.4311A>T	NP_001305758.1:p.Glu1437Asp
NM_001318831.2:c.3924A>T	NP_001305760.1:p.Glu1308Asp
NM_001318832.2:c.4488A>T	NP_001305761.1:p.Glu1496Asp
NM_001363528.2:c.4458A>T	NP_001350457.1:p.Glu1486Asp
NM_021055.3:c.4527A>T	NP_066399.2:p.Glu1509Asp