Canonical Allele Identifier: CA015107

Gene: TSC2

Linked Data

• ClinVar Variation Id: 64949
• ClinVar RCV Id: RCV000055152
• dbSNP Id: rs397514961
• MyVariant Identifiers: chr16:g.2114395_2114396dupCC (hg19) ; chr16:g.2064394_2064395dupCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2064394_2064395dup , CM000678.2:g.2064394_2064395dup	GRCh38
NC_000016.9:g.2114395_2114396dup , CM000678.1:g.2114395_2114396dup	GRCh37
NC_000016.8:g.2054396_2054397dup	NCBI36
NG_005895.1:g.20089_20090dup , LRG_487:g.20089_20090dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000568566.6:c.*113_*114dup	ENSP00000455997.2:n.*113_*114dup
ENST00000642206.2:c.1611_1612dup	ENSP00000495146.2:p.His538ProfsTer13
ENST00000642365.2:c.1566_1567dup	ENSP00000495459.2:p.His523ProfsTer13
ENST00000644417.2:c.*1003_*1004dup	ENSP00000493912.2:n.*1003_*1004dup
ENST00000646464.2:c.*1171_*1172dup	ENSP00000496610.2:n.*1171_*1172dup
ENST00000219476.9:c.1566_1567dup MANE Select	ENSP00000219476.3:p.His523ProfsTer13
ENST00000350773.9:c.1566_1567dup	ENSP00000344383.4:p.His523ProfsTer13
ENST00000401874.7:c.1566_1567dup	ENSP00000384468.2:p.His523ProfsTer13
ENST00000463601.2:n.1694_1695dup
ENST00000568454.6:c.1599_1600dup	ENSP00000454487.1:p.His534ProfsTer13
ENST00000642365.1:c.223_224dup
ENST00000642561.1:c.1566_1567dup	ENSP00000495099.1:p.His523ProfsTer13
ENST00000642797.1:c.1566_1567dup	ENSP00000493846.1:p.His523ProfsTer13
ENST00000642812.1:n.1611_1612dup
ENST00000642936.1:c.1566_1567dup	ENSP00000494514.1:p.His523ProfsTer13
ENST00000643088.1:c.1566_1567dup	ENSP00000494747.1:p.His523ProfsTer13
ENST00000643149.1:n.3576_3577dup
ENST00000643298.1:c.*1068_*1069dup	ENSP00000494393.1:n.*1068_*1069dup
ENST00000643745.1:c.*498_*499dup	ENSP00000495948.1:n.*498_*499dup
ENST00000643946.1:c.1566_1567dup	ENSP00000495927.1:p.His523ProfsTer13
ENST00000644043.1:c.1566_1567dup	ENSP00000496262.1:p.His523ProfsTer13
ENST00000644135.1:c.1566_1567dup	ENSP00000495644.1:p.His523ProfsTer13
ENST00000644222.1:n.1653_1654dup
ENST00000644329.1:c.1566_1567dup	ENSP00000496611.1:p.His523ProfsTer13
ENST00000644335.1:c.1566_1567dup	ENSP00000496317.1:p.His523ProfsTer13
ENST00000644399.1:c.1559_1560dup
ENST00000644665.1:n.2740_2741dup
ENST00000644847.1:n.558_559dup
ENST00000645591.1:n.2624_2625dup
ENST00000646388.1:c.1566_1567dup	ENSP00000495921.1:p.His523ProfsTer13
ENST00000646634.1:n.579_580dup
ENST00000647234.1:n.3324_3325dup
ENST00000647242.1:n.2202_2203dup
ENST00000219476.7:c.1566_1567dup	ENSP00000219476.3:p.His523ProfsTer13
ENST00000350773.8:c.1566_1567dup	ENSP00000344383.4:p.His523ProfsTer13
ENST00000382538.10:c.1419_1420dup	ENSP00000371978.6:p.His474ProfsTer13
ENST00000401874.6:c.1566_1567dup	ENSP00000384468.2:p.His523ProfsTer13
ENST00000439117.6:c.*865_*866dup	ENSP00000406980.2:n.*865_*866dup
ENST00000439673.6:c.1455_1456dup	ENSP00000399232.2:p.His486ProfsTer13
ENST00000490108.1:n.339_340dup
ENST00000568238.1:n.324_325dup
ENST00000568454.5:c.1599_1600dup	ENSP00000454487.1:p.His534ProfsTer13
ENST00000568566.5:c.206_207dup	ENSP00000455997.1:n.206_207dup
NM_000548.3:c.1566_1567dup , LRG_487t1:c.1566_1567dup	NP_000539.2:p.His523ProfsTer13
NM_001077183.1:c.1566_1567dup	NP_001070651.1:p.His523ProfsTer13
NM_001114382.1:c.1566_1567dup	NP_001107854.1:p.His523ProfsTer13
XM_005255529.3:c.1566_1567dup	XP_005255586.2:p.His523ProfsTer13
XM_005255531.3:c.1566_1567dup	XP_005255588.2:p.His523ProfsTer13
XM_011522636.1:c.1566_1567dup	XP_011520938.1:p.His523ProfsTer13
XM_011522637.1:c.1566_1567dup	XP_011520939.1:p.His523ProfsTer13
XM_011522638.1:c.1455_1456dup	XP_011520940.1:p.His486ProfsTer13
XM_011522639.1:c.1566_1567dup	XP_011520941.1:p.His523ProfsTer13
XM_011522640.1:c.1566_1567dup	XP_011520942.1:p.His523ProfsTer13
XM_011522641.1:c.1455_1456dup	XP_011520943.1:p.His486ProfsTer13
NM_000548.4:c.1566_1567dup	NP_000539.2:p.His523ProfsTer13
NM_001077183.2:c.1566_1567dup	NP_001070651.1:p.His523ProfsTer13
NM_001114382.2:c.1566_1567dup	NP_001107854.1:p.His523ProfsTer13
NM_001318827.1:c.1455_1456dup	NP_001305756.1:p.His486ProfsTer13
NM_001318829.1:c.1419_1420dup	NP_001305758.1:p.His474ProfsTer13
NM_001318831.1:c.966_967dup	NP_001305760.1:p.His323ProfsTer13
NM_001318832.1:c.1599_1600dup	NP_001305761.1:p.His534ProfsTer13
NM_001363528.1:c.1566_1567dup	NP_001350457.1:p.His523ProfsTer13
NM_021055.2:c.1566_1567dup	NP_066399.2:p.His523ProfsTer13
XM_005255531.4:c.1566_1567dup	XP_005255588.2:p.His523ProfsTer13
XM_011522636.2:c.1566_1567dup	XP_011520938.1:p.His523ProfsTer13
XM_011522637.2:c.1566_1567dup	XP_011520939.1:p.His523ProfsTer13
XM_011522638.2:c.1728_1729dup	XP_011520940.2:p.His577ProfsTer13
XM_011522639.2:c.1566_1567dup	XP_011520941.1:p.His523ProfsTer13
XM_011522640.2:c.1566_1567dup	XP_011520942.1:p.His523ProfsTer13
XM_017023615.1:c.1566_1567dup	XP_016879104.1:p.His523ProfsTer13
XM_017023616.1:c.1566_1567dup	XP_016879105.1:p.His523ProfsTer13
XM_017023617.1:c.1728_1729dup	XP_016879106.1:p.His577ProfsTer13
XM_017023618.1:c.222_223dup	XP_016879107.1:p.His75ProfsTer13
XM_024450413.1:c.1566_1567dup	XP_024306181.1:p.His523ProfsTer13
NM_000548.5:c.1566_1567dup MANE Select	NP_000539.2:p.His523ProfsTer13
NM_001370404.1:c.1566_1567dup	NP_001357333.1:p.His523ProfsTer13
NM_001370405.1:c.1566_1567dup	NP_001357334.1:p.His523ProfsTer13
NM_001077183.3:c.1566_1567dup	NP_001070651.1:p.His523ProfsTer13
NM_001114382.3:c.1566_1567dup	NP_001107854.1:p.His523ProfsTer13
NM_001318827.2:c.1455_1456dup	NP_001305756.1:p.His486ProfsTer13
NM_001318829.2:c.1419_1420dup	NP_001305758.1:p.His474ProfsTer13
NM_001318831.2:c.966_967dup	NP_001305760.1:p.His323ProfsTer13
NM_001318832.2:c.1599_1600dup	NP_001305761.1:p.His534ProfsTer13
NM_001363528.2:c.1566_1567dup	NP_001350457.1:p.His523ProfsTer13
NM_021055.3:c.1566_1567dup	NP_066399.2:p.His523ProfsTer13