Canonical Allele Identifier: CA019994

Gene: TSC2

Linked Data

• ClinVar Variation Id: 49497
• ClinVar RCV Id: RCV000042757 ; RCV001062658
• dbSNP Id: rs137854045
• MyVariant Identifiers: chr16:g.2134361C>T (hg19) ; chr16:g.2084360C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2084360C>T , CM000678.2:g.2084360C>T	GRCh38
NC_000016.9:g.2134361C>T , CM000678.1:g.2134361C>T	GRCh37
NC_000016.8:g.2074362C>T	NCBI36
NG_005895.1:g.40055C>T , LRG_487:g.40055C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*2487C>T	ENSP00000455997.2:n.*2487C>T
ENST00000642206.2:c.3985C>T	ENSP00000495146.2:p.Gln1329Ter
ENST00000642365.2:c.4135C>T	ENSP00000495459.2:p.Gln1379Ter
ENST00000644417.2:c.*4518C>T	ENSP00000493912.2:n.*4518C>T
ENST00000646464.2:c.*6887C>T	ENSP00000496610.2:n.*6887C>T
ENST00000219476.9:c.4138C>T MANE Select	ENSP00000219476.3:p.Gln1380Ter
ENST00000350773.9:c.4069C>T	ENSP00000344383.4:p.Gln1357Ter
ENST00000401874.7:c.3937C>T	ENSP00000384468.2:p.Gln1313Ter
ENST00000568454.6:c.3970C>T	ENSP00000454487.1:p.Gln1324Ter
ENST00000569110.2:c.374C>T
ENST00000569930.2:n.2020C>T
ENST00000642365.1:c.2792C>T
ENST00000642561.1:c.4009C>T	ENSP00000495099.1:p.Gln1337Ter
ENST00000642728.1:n.320C>T
ENST00000642797.1:c.3940C>T	ENSP00000493846.1:p.Gln1314Ter
ENST00000642936.1:c.4006C>T	ENSP00000494514.1:p.Gln1336Ter
ENST00000643088.1:c.3937C>T	ENSP00000494747.1:p.Gln1313Ter
ENST00000643177.1:n.152C>T
ENST00000643426.1:n.1786C>T
ENST00000643946.1:c.4069C>T	ENSP00000495927.1:p.Gln1357Ter
ENST00000644043.1:c.4009C>T	ENSP00000496262.1:p.Gln1337Ter
ENST00000644329.1:c.3937C>T	ENSP00000496611.1:p.Gln1313Ter
ENST00000644335.1:c.3940C>T	ENSP00000496317.1:p.Gln1314Ter
ENST00000644399.1:c.4059C>T
ENST00000645024.1:n.2222C>T
ENST00000645186.1:c.381C>T
ENST00000646388.1:c.4138C>T	ENSP00000495921.1:p.Gln1380Ter
ENST00000646634.1:n.2953C>T
ENST00000646674.1:n.1390C>T
ENST00000647042.1:n.1361C>T
ENST00000647180.1:n.1251C>T
ENST00000219476.7:c.4138C>T	ENSP00000219476.3:p.Gln1380Ter
ENST00000350773.8:c.4069C>T	ENSP00000344383.4:p.Gln1357Ter
ENST00000382538.10:c.3793C>T	ENSP00000371978.6:p.Gln1265Ter
ENST00000401874.6:c.3937C>T	ENSP00000384468.2:p.Gln1313Ter
ENST00000439117.6:c.*3305C>T	ENSP00000406980.2:n.*3305C>T
ENST00000439673.6:c.3829C>T	ENSP00000399232.2:p.Gln1277Ter
ENST00000497886.5:n.1896C>T
ENST00000568454.5:c.3970C>T	ENSP00000454487.1:p.Gln1324Ter
ENST00000569110.1:c.320C>T
ENST00000569930.1:n.1253C>T
NM_000548.3:c.4138C>T , LRG_487t1:c.4138C>T	NP_000539.2:p.Gln1380Ter
NM_001077183.1:c.3937C>T	NP_001070651.1:p.Gln1313Ter
NM_001114382.1:c.4069C>T	NP_001107854.1:p.Gln1357Ter
XM_005255529.3:c.4009C>T	XP_005255586.2:p.Gln1337Ter
XM_005255531.3:c.3940C>T	XP_005255588.2:p.Gln1314Ter
XM_011522636.1:c.4192C>T	XP_011520938.1:p.Gln1398Ter
XM_011522637.1:c.4189C>T	XP_011520939.1:p.Gln1397Ter
XM_011522638.1:c.4081C>T	XP_011520940.1:p.Gln1361Ter
XM_011522639.1:c.4063C>T	XP_011520941.1:p.Gln1355Ter
XM_011522640.1:c.4060C>T	XP_011520942.1:p.Gln1354Ter
XM_011522641.1:c.3829C>T	XP_011520943.1:p.Gln1277Ter
NM_000548.4:c.4138C>T	NP_000539.2:p.Gln1380Ter
NM_001077183.2:c.3937C>T	NP_001070651.1:p.Gln1313Ter
NM_001114382.2:c.4069C>T	NP_001107854.1:p.Gln1357Ter
NM_001318827.1:c.3829C>T	NP_001305756.1:p.Gln1277Ter
NM_001318829.1:c.3793C>T	NP_001305758.1:p.Gln1265Ter
NM_001318831.1:c.3406C>T	NP_001305760.1:p.Gln1136Ter
NM_001318832.1:c.3970C>T	NP_001305761.1:p.Gln1324Ter
NM_001363528.1:c.3940C>T	NP_001350457.1:p.Gln1314Ter
NM_021055.2:c.4009C>T	NP_066399.2:p.Gln1337Ter
XM_005255531.4:c.3940C>T	XP_005255588.2:p.Gln1314Ter
XM_011522636.2:c.4192C>T	XP_011520938.1:p.Gln1398Ter
XM_011522637.2:c.4189C>T	XP_011520939.1:p.Gln1397Ter
XM_011522638.2:c.4354C>T	XP_011520940.2:p.Gln1452Ter
XM_011522639.2:c.4063C>T	XP_011520941.1:p.Gln1355Ter
XM_011522640.2:c.4060C>T	XP_011520942.1:p.Gln1354Ter
XM_017023615.1:c.4135C>T	XP_016879104.1:p.Gln1379Ter
XM_017023616.1:c.4006C>T	XP_016879105.1:p.Gln1336Ter
XM_017023617.1:c.4102C>T	XP_016879106.1:p.Gln1368Ter
XM_017023618.1:c.2848C>T	XP_016879107.1:p.Gln950Ter
XM_024450413.1:c.3937C>T	XP_024306181.1:p.Gln1313Ter
NM_000548.5:c.4138C>T MANE Select	NP_000539.2:p.Gln1380Ter
NM_001370404.1:c.4006C>T	NP_001357333.1:p.Gln1336Ter
NM_001370405.1:c.4009C>T	NP_001357334.1:p.Gln1337Ter
NM_001077183.3:c.3937C>T	NP_001070651.1:p.Gln1313Ter
NM_001114382.3:c.4069C>T	NP_001107854.1:p.Gln1357Ter
NM_001318827.2:c.3829C>T	NP_001305756.1:p.Gln1277Ter
NM_001318829.2:c.3793C>T	NP_001305758.1:p.Gln1265Ter
NM_001318831.2:c.3406C>T	NP_001305760.1:p.Gln1136Ter
NM_001318832.2:c.3970C>T	NP_001305761.1:p.Gln1324Ter
NM_001363528.2:c.3940C>T	NP_001350457.1:p.Gln1314Ter
NM_021055.3:c.4009C>T	NP_066399.2:p.Gln1337Ter