Canonical Allele Identifier: CA2202031881

Gene: TSC2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2088262C= , CM000678.2:g.2088262C=	GRCh38
NC_000016.9:g.2138263C= , CM000678.1:g.2138263C=	GRCh37
NC_000016.8:g.2078264C=	NCBI36
NG_005895.1:g.43957C= , LRG_487:g.43957C=
NG_008617.1:g.54959G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*3545C=	ENSP00000455997.2:n.*3545C=
ENST00000642206.2:c.5043C=	ENSP00000495146.2:p.Pro1681=
ENST00000642365.2:c.5193C=	ENSP00000495459.2:p.Pro1731=
ENST00000644417.2:c.*5709C=	ENSP00000493912.2:n.*5709C=
ENST00000646464.2:c.*7945C=	ENSP00000496610.2:n.*7945C=
ENST00000219476.9:c.5196C= MANE Select	ENSP00000219476.3:p.Pro1732=
ENST00000350773.9:c.5127C=	ENSP00000344383.4:p.Pro1709=
ENST00000401874.7:c.4995C=	ENSP00000384468.2:p.Pro1665=
ENST00000568454.6:c.5028C=	ENSP00000454487.1:p.Pro1676=
ENST00000569110.2:c.1419C=
ENST00000569930.2:n.3078C=
ENST00000642365.1:c.3850C=
ENST00000642561.1:c.5055C=	ENSP00000495099.1:p.Pro1685=
ENST00000642791.1:n.793C=
ENST00000642797.1:c.4998C=	ENSP00000493846.1:p.Pro1666=
ENST00000642936.1:c.5064C=	ENSP00000494514.1:p.Pro1688=
ENST00000643088.1:c.4989C=	ENSP00000494747.1:p.Pro1663=
ENST00000643426.1:n.2844C=
ENST00000643946.1:c.5121C=	ENSP00000495927.1:p.Pro1707=
ENST00000644043.1:c.5067C=	ENSP00000496262.1:p.Pro1689=
ENST00000644329.1:c.5082C=	ENSP00000496611.1:p.Pro1694=
ENST00000644335.1:c.4992C=	ENSP00000496317.1:p.Pro1664=
ENST00000644399.1:c.5117C=
ENST00000645024.1:n.3280C=
ENST00000646388.1:c.5190C=	ENSP00000495921.1:p.Pro1730=
ENST00000646634.1:n.4011C=
ENST00000646674.1:n.2448C=
ENST00000647042.1:n.2419C=
ENST00000647180.1:n.2309C=
ENST00000219476.7:c.5196C=	ENSP00000219476.3:p.Pro1732=
ENST00000350773.8:c.5127C=	ENSP00000344383.4:p.Pro1709=
ENST00000382538.10:c.4851C=	ENSP00000371978.6:p.Pro1617=
ENST00000401874.6:c.4995C=	ENSP00000384468.2:p.Pro1665=
ENST00000439117.6:c.*4363C=	ENSP00000406980.2:n.*4363C=
ENST00000439673.6:c.4887C=	ENSP00000399232.2:p.Pro1629=
ENST00000497886.5:n.2919C=
ENST00000568454.5:c.5028C=	ENSP00000454487.1:p.Pro1676=
ENST00000569110.1:c.1378C=
ENST00000569930.1:n.2311C=
NM_000548.3:c.5196C= , LRG_487t1:c.5196C=	NP_000539.2:p.Pro1732=
NM_001077183.1:c.4995C=	NP_001070651.1:p.Pro1665=
NM_001114382.1:c.5127C=	NP_001107854.1:p.Pro1709=
XM_005255529.3:c.5067C=	XP_005255586.2:p.Pro1689=
XM_005255531.3:c.4998C=	XP_005255588.2:p.Pro1666=
XM_011522636.1:c.5250C=	XP_011520938.1:p.Pro1750=
XM_011522637.1:c.5247C=	XP_011520939.1:p.Pro1749=
XM_011522638.1:c.5139C=	XP_011520940.1:p.Pro1713=
XM_011522639.1:c.5121C=	XP_011520941.1:p.Pro1707=
XM_011522640.1:c.5118C=	XP_011520942.1:p.Pro1706=
XM_011522641.1:c.4887C=	XP_011520943.1:p.Pro1629=
NM_000548.4:c.5196C=	NP_000539.2:p.Pro1732=
NM_001077183.2:c.4995C=	NP_001070651.1:p.Pro1665=
NM_001114382.2:c.5127C=	NP_001107854.1:p.Pro1709=
NM_001318827.1:c.4887C=	NP_001305756.1:p.Pro1629=
NM_001318829.1:c.4851C=	NP_001305758.1:p.Pro1617=
NM_001318831.1:c.4464C=	NP_001305760.1:p.Pro1488=
NM_001318832.1:c.5028C=	NP_001305761.1:p.Pro1676=
NM_001363528.1:c.4998C=	NP_001350457.1:p.Pro1666=
NM_021055.2:c.5067C=	NP_066399.2:p.Pro1689=
XM_005255531.4:c.4998C=	XP_005255588.2:p.Pro1666=
XM_011522636.2:c.5250C=	XP_011520938.1:p.Pro1750=
XM_011522637.2:c.5247C=	XP_011520939.1:p.Pro1749=
XM_011522638.2:c.5412C=	XP_011520940.2:p.Pro1804=
XM_011522639.2:c.5121C=	XP_011520941.1:p.Pro1707=
XM_011522640.2:c.5118C=	XP_011520942.1:p.Pro1706=
XM_017023615.1:c.5193C=	XP_016879104.1:p.Pro1731=
XM_017023616.1:c.5064C=	XP_016879105.1:p.Pro1688=
XM_017023617.1:c.5160C=	XP_016879106.1:p.Pro1720=
XM_017023618.1:c.3906C=	XP_016879107.1:p.Pro1302=
XM_024450413.1:c.5082C=	XP_024306181.1:p.Pro1694=
NM_000548.5:c.5196C= MANE Select	NP_000539.2:p.Pro1732=
NM_001370404.1:c.5064C=	NP_001357333.1:p.Pro1688=
NM_001370405.1:c.5055C=	NP_001357334.1:p.Pro1685=
NM_001077183.3:c.4995C=	NP_001070651.1:p.Pro1665=
NM_001114382.3:c.5127C=	NP_001107854.1:p.Pro1709=
NM_001318827.2:c.4887C=	NP_001305756.1:p.Pro1629=
NM_001318829.2:c.4851C=	NP_001305758.1:p.Pro1617=
NM_001318831.2:c.4464C=	NP_001305760.1:p.Pro1488=
NM_001318832.2:c.5028C=	NP_001305761.1:p.Pro1676=
NM_001363528.2:c.4998C=	NP_001350457.1:p.Pro1666=
NM_021055.3:c.5067C=	NP_066399.2:p.Pro1689=