Canonical Allele Identifier: CA394302113

Gene: TSC2

Linked Data

• ClinVar Variation Id: 1038017
• ClinVar RCV Id: RCV001341263
• dbSNP Id: rs2090534118
• gnomAD v4: 16-2084637-G-T
• MyVariant Identifiers: chr16:g.2134638G>T (hg19) ; chr16:g.2084637G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2084637G>T , CM000678.2:g.2084637G>T	GRCh38
NC_000016.9:g.2134638G>T , CM000678.1:g.2134638G>T	GRCh37
NC_000016.8:g.2074639G>T	NCBI36
NG_005895.1:g.40332G>T , LRG_487:g.40332G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000568566.6:c.*2764G>T	ENSP00000455997.2:n.*2764G>T
ENST00000642206.2:c.4262G>T	ENSP00000495146.2:p.Gly1421Val
ENST00000642365.2:c.4412G>T	ENSP00000495459.2:p.Gly1471Val
ENST00000644417.2:c.*4795G>T	ENSP00000493912.2:n.*4795G>T
ENST00000646464.2:c.*7164G>T	ENSP00000496610.2:n.*7164G>T
ENST00000219476.9:c.4415G>T MANE Select	ENSP00000219476.3:p.Gly1472Val
ENST00000350773.9:c.4346G>T	ENSP00000344383.4:p.Gly1449Val
ENST00000401874.7:c.4214G>T	ENSP00000384468.2:p.Gly1405Val
ENST00000568454.6:c.4247G>T	ENSP00000454487.1:p.Gly1416Val
ENST00000569110.2:c.651G>T
ENST00000569930.2:n.2297G>T
ENST00000642365.1:c.3069G>T
ENST00000642561.1:c.4286G>T	ENSP00000495099.1:p.Gly1429Val
ENST00000642728.1:n.597G>T
ENST00000642797.1:c.4217G>T	ENSP00000493846.1:p.Gly1406Val
ENST00000642936.1:c.4283G>T	ENSP00000494514.1:p.Gly1428Val
ENST00000643088.1:c.4214G>T	ENSP00000494747.1:p.Gly1405Val
ENST00000643177.1:n.429G>T
ENST00000643426.1:n.2063G>T
ENST00000643946.1:c.4346G>T	ENSP00000495927.1:p.Gly1449Val
ENST00000644043.1:c.4286G>T	ENSP00000496262.1:p.Gly1429Val
ENST00000644329.1:c.4214G>T	ENSP00000496611.1:p.Gly1405Val
ENST00000644335.1:c.4217G>T	ENSP00000496317.1:p.Gly1406Val
ENST00000644399.1:c.4336G>T
ENST00000645024.1:n.2499G>T
ENST00000646388.1:c.4415G>T	ENSP00000495921.1:p.Gly1472Val
ENST00000646634.1:n.3230G>T
ENST00000646674.1:n.1667G>T
ENST00000647042.1:n.1638G>T
ENST00000647180.1:n.1528G>T
ENST00000219476.7:c.4415G>T	ENSP00000219476.3:p.Gly1472Val
ENST00000350773.8:c.4346G>T	ENSP00000344383.4:p.Gly1449Val
ENST00000382538.10:c.4070G>T	ENSP00000371978.6:p.Gly1357Val
ENST00000401874.6:c.4214G>T	ENSP00000384468.2:p.Gly1405Val
ENST00000439117.6:c.*3582G>T	ENSP00000406980.2:n.*3582G>T
ENST00000439673.6:c.4106G>T	ENSP00000399232.2:p.Gly1369Val
ENST00000497886.5:n.2173G>T
ENST00000568454.5:c.4247G>T	ENSP00000454487.1:p.Gly1416Val
ENST00000569110.1:c.597G>T
ENST00000569930.1:n.1530G>T
NM_000548.3:c.4415G>T , LRG_487t1:c.4415G>T	NP_000539.2:p.Gly1472Val
NM_001077183.1:c.4214G>T	NP_001070651.1:p.Gly1405Val
NM_001114382.1:c.4346G>T	NP_001107854.1:p.Gly1449Val
XM_005255529.3:c.4286G>T	XP_005255586.2:p.Gly1429Val
XM_005255531.3:c.4217G>T	XP_005255588.2:p.Gly1406Val
XM_011522636.1:c.4469G>T	XP_011520938.1:p.Gly1490Val
XM_011522637.1:c.4466G>T	XP_011520939.1:p.Gly1489Val
XM_011522638.1:c.4358G>T	XP_011520940.1:p.Gly1453Val
XM_011522639.1:c.4340G>T	XP_011520941.1:p.Gly1447Val
XM_011522640.1:c.4337G>T	XP_011520942.1:p.Gly1446Val
XM_011522641.1:c.4106G>T	XP_011520943.1:p.Gly1369Val
NM_000548.4:c.4415G>T	NP_000539.2:p.Gly1472Val
NM_001077183.2:c.4214G>T	NP_001070651.1:p.Gly1405Val
NM_001114382.2:c.4346G>T	NP_001107854.1:p.Gly1449Val
NM_001318827.1:c.4106G>T	NP_001305756.1:p.Gly1369Val
NM_001318829.1:c.4070G>T	NP_001305758.1:p.Gly1357Val
NM_001318831.1:c.3683G>T	NP_001305760.1:p.Gly1228Val
NM_001318832.1:c.4247G>T	NP_001305761.1:p.Gly1416Val
NM_001363528.1:c.4217G>T	NP_001350457.1:p.Gly1406Val
NM_021055.2:c.4286G>T	NP_066399.2:p.Gly1429Val
XM_005255531.4:c.4217G>T	XP_005255588.2:p.Gly1406Val
XM_011522636.2:c.4469G>T	XP_011520938.1:p.Gly1490Val
XM_011522637.2:c.4466G>T	XP_011520939.1:p.Gly1489Val
XM_011522638.2:c.4631G>T	XP_011520940.2:p.Gly1544Val
XM_011522639.2:c.4340G>T	XP_011520941.1:p.Gly1447Val
XM_011522640.2:c.4337G>T	XP_011520942.1:p.Gly1446Val
XM_017023615.1:c.4412G>T	XP_016879104.1:p.Gly1471Val
XM_017023616.1:c.4283G>T	XP_016879105.1:p.Gly1428Val
XM_017023617.1:c.4379G>T	XP_016879106.1:p.Gly1460Val
XM_017023618.1:c.3125G>T	XP_016879107.1:p.Gly1042Val
XM_024450413.1:c.4214G>T	XP_024306181.1:p.Gly1405Val
NM_000548.5:c.4415G>T MANE Select	NP_000539.2:p.Gly1472Val
NM_001370404.1:c.4283G>T	NP_001357333.1:p.Gly1428Val
NM_001370405.1:c.4286G>T	NP_001357334.1:p.Gly1429Val
NM_001077183.3:c.4214G>T	NP_001070651.1:p.Gly1405Val
NM_001114382.3:c.4346G>T	NP_001107854.1:p.Gly1449Val
NM_001318827.2:c.4106G>T	NP_001305756.1:p.Gly1369Val
NM_001318829.2:c.4070G>T	NP_001305758.1:p.Gly1357Val
NM_001318831.2:c.3683G>T	NP_001305760.1:p.Gly1228Val
NM_001318832.2:c.4247G>T	NP_001305761.1:p.Gly1416Val
NM_001363528.2:c.4217G>T	NP_001350457.1:p.Gly1406Val
NM_021055.3:c.4286G>T	NP_066399.2:p.Gly1429Val