Canonical Allele Identifier: CA276759574

Gene: TSC2

Linked Data

• ClinVar Variation Id: 1967322
• ClinVar RCV Id: RCV002721955
• dbSNP Id: rs370353005
• MyVariant Identifiers: chr16:g.2138317C>T (hg19) ; chr16:g.2088316C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2088316C>T , CM000678.2:g.2088316C>T	GRCh38
NC_000016.9:g.2138317C>T , CM000678.1:g.2138317C>T	GRCh37
NC_000016.8:g.2078318C>T	NCBI36
NG_005895.1:g.44011C>T , LRG_487:g.44011C>T
NG_008617.1:g.54905G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*3599C>T	ENSP00000455997.2:n.*3599C>T
ENST00000642206.2:c.5097C>T	ENSP00000495146.2:p.Leu1699=
ENST00000642365.2:c.5247C>T	ENSP00000495459.2:p.Leu1749=
ENST00000644417.2:c.*5763C>T	ENSP00000493912.2:n.*5763C>T
ENST00000646464.2:c.*7999C>T	ENSP00000496610.2:n.*7999C>T
ENST00000219476.9:c.5250C>T MANE Select	ENSP00000219476.3:p.Leu1750=
ENST00000350773.9:c.5181C>T	ENSP00000344383.4:p.Leu1727=
ENST00000401874.7:c.5049C>T	ENSP00000384468.2:p.Leu1683=
ENST00000568454.6:c.5082C>T	ENSP00000454487.1:p.Leu1694=
ENST00000569110.2:c.1473C>T
ENST00000569930.2:n.3132C>T
ENST00000642365.1:c.3904C>T
ENST00000642561.1:c.5109C>T	ENSP00000495099.1:p.Leu1703=
ENST00000642791.1:n.847C>T
ENST00000642797.1:c.5052C>T	ENSP00000493846.1:p.Leu1684=
ENST00000642936.1:c.5118C>T	ENSP00000494514.1:p.Leu1706=
ENST00000643088.1:c.5043C>T	ENSP00000494747.1:p.Leu1681=
ENST00000643426.1:n.2898C>T
ENST00000643946.1:c.5175C>T	ENSP00000495927.1:p.Leu1725=
ENST00000644043.1:c.5121C>T	ENSP00000496262.1:p.Leu1707=
ENST00000644329.1:c.5136C>T	ENSP00000496611.1:p.Leu1712=
ENST00000644335.1:c.5046C>T	ENSP00000496317.1:p.Leu1682=
ENST00000644399.1:c.5171C>T
ENST00000645024.1:n.3334C>T
ENST00000646388.1:c.5244C>T	ENSP00000495921.1:p.Leu1748=
ENST00000646634.1:n.4065C>T
ENST00000646674.1:n.2502C>T
ENST00000647042.1:n.2473C>T
ENST00000647180.1:n.2363C>T
ENST00000219476.7:c.5250C>T	ENSP00000219476.3:p.Leu1750=
ENST00000350773.8:c.5181C>T	ENSP00000344383.4:p.Leu1727=
ENST00000382538.10:c.4905C>T	ENSP00000371978.6:p.Leu1635=
ENST00000401874.6:c.5049C>T	ENSP00000384468.2:p.Leu1683=
ENST00000439117.6:c.*4417C>T	ENSP00000406980.2:n.*4417C>T
ENST00000439673.6:c.4941C>T	ENSP00000399232.2:p.Leu1647=
ENST00000497886.5:n.2973C>T
ENST00000568454.5:c.5082C>T	ENSP00000454487.1:p.Leu1694=
ENST00000569110.1:c.1432C>T
ENST00000569930.1:n.2365C>T
NM_000548.3:c.5250C>T , LRG_487t1:c.5250C>T	NP_000539.2:p.Leu1750=
NM_001077183.1:c.5049C>T	NP_001070651.1:p.Leu1683=
NM_001114382.1:c.5181C>T	NP_001107854.1:p.Leu1727=
XM_005255529.3:c.5121C>T	XP_005255586.2:p.Leu1707=
XM_005255531.3:c.5052C>T	XP_005255588.2:p.Leu1684=
XM_011522636.1:c.5304C>T	XP_011520938.1:p.Leu1768=
XM_011522637.1:c.5301C>T	XP_011520939.1:p.Leu1767=
XM_011522638.1:c.5193C>T	XP_011520940.1:p.Leu1731=
XM_011522639.1:c.5175C>T	XP_011520941.1:p.Leu1725=
XM_011522640.1:c.5172C>T	XP_011520942.1:p.Leu1724=
XM_011522641.1:c.4941C>T	XP_011520943.1:p.Leu1647=
NM_000548.4:c.5250C>T	NP_000539.2:p.Leu1750=
NM_001077183.2:c.5049C>T	NP_001070651.1:p.Leu1683=
NM_001114382.2:c.5181C>T	NP_001107854.1:p.Leu1727=
NM_001318827.1:c.4941C>T	NP_001305756.1:p.Leu1647=
NM_001318829.1:c.4905C>T	NP_001305758.1:p.Leu1635=
NM_001318831.1:c.4518C>T	NP_001305760.1:p.Leu1506=
NM_001318832.1:c.5082C>T	NP_001305761.1:p.Leu1694=
NM_001363528.1:c.5052C>T	NP_001350457.1:p.Leu1684=
NM_021055.2:c.5121C>T	NP_066399.2:p.Leu1707=
XM_005255531.4:c.5052C>T	XP_005255588.2:p.Leu1684=
XM_011522636.2:c.5304C>T	XP_011520938.1:p.Leu1768=
XM_011522637.2:c.5301C>T	XP_011520939.1:p.Leu1767=
XM_011522638.2:c.5466C>T	XP_011520940.2:p.Leu1822=
XM_011522639.2:c.5175C>T	XP_011520941.1:p.Leu1725=
XM_011522640.2:c.5172C>T	XP_011520942.1:p.Leu1724=
XM_017023615.1:c.5247C>T	XP_016879104.1:p.Leu1749=
XM_017023616.1:c.5118C>T	XP_016879105.1:p.Leu1706=
XM_017023617.1:c.5214C>T	XP_016879106.1:p.Leu1738=
XM_017023618.1:c.3960C>T	XP_016879107.1:p.Leu1320=
XM_024450413.1:c.5136C>T	XP_024306181.1:p.Leu1712=
NM_000548.5:c.5250C>T MANE Select	NP_000539.2:p.Leu1750=
NM_001370404.1:c.5118C>T	NP_001357333.1:p.Leu1706=
NM_001370405.1:c.5109C>T	NP_001357334.1:p.Leu1703=
NM_001077183.3:c.5049C>T	NP_001070651.1:p.Leu1683=
NM_001114382.3:c.5181C>T	NP_001107854.1:p.Leu1727=
NM_001318827.2:c.4941C>T	NP_001305756.1:p.Leu1647=
NM_001318829.2:c.4905C>T	NP_001305758.1:p.Leu1635=
NM_001318831.2:c.4518C>T	NP_001305760.1:p.Leu1506=
NM_001318832.2:c.5082C>T	NP_001305761.1:p.Leu1694=
NM_001363528.2:c.5052C>T	NP_001350457.1:p.Leu1684=
NM_021055.3:c.5121C>T	NP_066399.2:p.Leu1707=