Canonical Allele Identifier: CA021717

Gene: TSC2

Linked Data

• ClinVar Variation Id: 65314
• ClinVar RCV Id: RCV000055537
• dbSNP Id: rs397515229
• MyVariant Identifiers: chr16:g.2105430_2105431insAT (hg19) ; chr16:g.2055429_2055430insAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2055429_2055430insAT , CM000678.2:g.2055429_2055430insAT	GRCh38
NC_000016.9:g.2105430_2105431insAT , CM000678.1:g.2105430_2105431insAT	GRCh37
NC_000016.8:g.2045431_2045432insAT	NCBI36
NG_005895.1:g.11124_11125insAT , LRG_487:g.11124_11125insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.509_510insAT	ENSP00000455997.2:p.Gly171LeufsTer12
ENST00000642206.2:c.554_555insAT	ENSP00000495146.2:p.Gly186LeufsTer12
ENST00000642365.2:c.509_510insAT	ENSP00000495459.2:p.Gly171LeufsTer12
ENST00000644417.2:c.492_493insAT	ENSP00000493912.2:p.Trp165IlefsTer?
ENST00000646464.2:c.226-551_226-550insAT	ENSP00000496610.2:n.226-551_226-550insAT
ENST00000219476.9:c.509_510insAT MANE Select	ENSP00000219476.3:p.Gly171LeufsTer12
ENST00000350773.9:c.509_510insAT	ENSP00000344383.4:p.Gly171LeufsTer12
ENST00000401874.7:c.509_510insAT	ENSP00000384468.2:p.Gly171LeufsTer12
ENST00000432909.3:c.283_284insAT
ENST00000461648.3:n.2423_2424insAT
ENST00000568454.6:c.542_543insAT	ENSP00000454487.1:p.Gly182LeufsTer12
ENST00000568692.2:n.1232_1233insAT
ENST00000642561.1:c.509_510insAT	ENSP00000495099.1:p.Gly171LeufsTer12
ENST00000642797.1:c.509_510insAT	ENSP00000493846.1:p.Gly171LeufsTer12
ENST00000642812.1:n.566_567insAT
ENST00000642936.1:c.509_510insAT	ENSP00000494514.1:p.Gly171LeufsTer12
ENST00000643088.1:c.509_510insAT	ENSP00000494747.1:p.Gly171LeufsTer12
ENST00000643120.1:n.533_534insAT
ENST00000643149.1:n.1462_1463insAT
ENST00000643298.1:c.509_510insAT	ENSP00000494393.1:p.Gly171LeufsTer12
ENST00000643745.1:c.509_510insAT	ENSP00000495948.1:p.Gly171LeufsTer12
ENST00000643946.1:c.509_510insAT	ENSP00000495927.1:p.Gly171LeufsTer12
ENST00000644043.1:c.509_510insAT	ENSP00000496262.1:p.Gly171LeufsTer12
ENST00000644135.1:c.509_510insAT	ENSP00000495644.1:p.Gly171LeufsTer12
ENST00000644222.1:n.596_597insAT
ENST00000644329.1:c.509_510insAT	ENSP00000496611.1:p.Gly171LeufsTer12
ENST00000644335.1:c.509_510insAT	ENSP00000496317.1:p.Gly171LeufsTer12
ENST00000644399.1:c.502_503insAT
ENST00000644417.1:c.207_208insAT	ENSP00000493912.1:p.Trp70IlefsTer?
ENST00000644665.1:n.626_627insAT
ENST00000645591.1:n.1480_1481insAT
ENST00000646388.1:c.509_510insAT	ENSP00000495921.1:p.Gly171LeufsTer12
ENST00000646823.1:n.897_898insAT
ENST00000647234.1:n.1210_1211insAT
ENST00000647242.1:n.1177_1178insAT
ENST00000219476.7:c.509_510insAT	ENSP00000219476.3:p.Gly171LeufsTer12
ENST00000350773.8:c.509_510insAT	ENSP00000344383.4:p.Gly171LeufsTer12
ENST00000382538.10:c.362_363insAT	ENSP00000371978.6:p.Gly122LeufsTer12
ENST00000401874.6:c.509_510insAT	ENSP00000384468.2:p.Gly171LeufsTer12
ENST00000432909.2:c.283_284insAT
ENST00000439117.6:c.226-767_226-766insAT	ENSP00000406980.2:n.226-767_226-766insAT
ENST00000439673.6:c.398_399insAT	ENSP00000399232.2:p.Gly134LeufsTer12
ENST00000568454.5:c.542_543insAT	ENSP00000454487.1:p.Gly182LeufsTer12
ENST00000568692.1:n.173_174insAT
NM_000548.3:c.509_510insAT , LRG_487t1:c.509_510insAT	NP_000539.2:p.Gly171LeufsTer12
NM_001077183.1:c.509_510insAT	NP_001070651.1:p.Gly171LeufsTer12
NM_001114382.1:c.509_510insAT	NP_001107854.1:p.Gly171LeufsTer12
XM_005255529.3:c.509_510insAT	XP_005255586.2:p.Gly171LeufsTer12
XM_005255531.3:c.509_510insAT	XP_005255588.2:p.Gly171LeufsTer12
XM_011522636.1:c.509_510insAT	XP_011520938.1:p.Gly171LeufsTer12
XM_011522637.1:c.509_510insAT	XP_011520939.1:p.Gly171LeufsTer12
XM_011522638.1:c.398_399insAT	XP_011520940.1:p.Gly134LeufsTer12
XM_011522639.1:c.509_510insAT	XP_011520941.1:p.Gly171LeufsTer12
XM_011522640.1:c.509_510insAT	XP_011520942.1:p.Gly171LeufsTer12
XM_011522641.1:c.398_399insAT	XP_011520943.1:p.Gly134LeufsTer12
NM_000548.4:c.509_510insAT	NP_000539.2:p.Gly171LeufsTer12
NM_001077183.2:c.509_510insAT	NP_001070651.1:p.Gly171LeufsTer12
NM_001114382.2:c.509_510insAT	NP_001107854.1:p.Gly171LeufsTer12
NM_001318827.1:c.398_399insAT	NP_001305756.1:p.Gly134LeufsTer12
NM_001318829.1:c.362_363insAT	NP_001305758.1:p.Gly122LeufsTer12
NM_001318831.1:c.-1-767_-1-766insAT	NP_001305760.1:n.-1-767_-1-766insAT
NM_001318832.1:c.542_543insAT	NP_001305761.1:p.Gly182LeufsTer12
NM_001363528.1:c.509_510insAT	NP_001350457.1:p.Gly171LeufsTer12
NM_021055.2:c.509_510insAT	NP_066399.2:p.Gly171LeufsTer12
XM_005255531.4:c.509_510insAT	XP_005255588.2:p.Gly171LeufsTer12
XM_011522636.2:c.509_510insAT	XP_011520938.1:p.Gly171LeufsTer12
XM_011522637.2:c.509_510insAT	XP_011520939.1:p.Gly171LeufsTer12
XM_011522638.2:c.671_672insAT	XP_011520940.2:p.Gly225LeufsTer12
XM_011522639.2:c.509_510insAT	XP_011520941.1:p.Gly171LeufsTer12
XM_011522640.2:c.509_510insAT	XP_011520942.1:p.Gly171LeufsTer12
XM_017023615.1:c.509_510insAT	XP_016879104.1:p.Gly171LeufsTer12
XM_017023616.1:c.509_510insAT	XP_016879105.1:p.Gly171LeufsTer12
XM_017023617.1:c.671_672insAT	XP_016879106.1:p.Gly225LeufsTer12
XM_017023618.1:c.-923_-922insAT	XP_016879107.1:n.-923_-922insAT
XM_024450413.1:c.509_510insAT	XP_024306181.1:p.Gly171LeufsTer12
NM_000548.5:c.509_510insAT MANE Select	NP_000539.2:p.Gly171LeufsTer12
NM_001370404.1:c.509_510insAT	NP_001357333.1:p.Gly171LeufsTer12
NM_001370405.1:c.509_510insAT	NP_001357334.1:p.Gly171LeufsTer12
NM_001077183.3:c.509_510insAT	NP_001070651.1:p.Gly171LeufsTer12
NM_001114382.3:c.509_510insAT	NP_001107854.1:p.Gly171LeufsTer12
NM_001318827.2:c.398_399insAT	NP_001305756.1:p.Gly134LeufsTer12
NM_001318829.2:c.362_363insAT	NP_001305758.1:p.Gly122LeufsTer12
NM_001318831.2:c.-1-767_-1-766insAT	NP_001305760.1:n.-1-767_-1-766insAT
NM_001318832.2:c.542_543insAT	NP_001305761.1:p.Gly182LeufsTer12
NM_001363528.2:c.509_510insAT	NP_001350457.1:p.Gly171LeufsTer12
NM_021055.3:c.509_510insAT	NP_066399.2:p.Gly171LeufsTer12