Canonical Allele Identifier: CA2202019093
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2085237C= , CM000678.2:g.2085237C= GRCh38
NC_000016.9:g.2135238C= , CM000678.1:g.2135238C= GRCh37
NC_000016.8:g.2075239C= NCBI36
NG_005895.1:g.40932C= , LRG_487:g.40932C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*2926C= ENSP00000455997.2:n.*2926C=
ENST00000642206.2:c.4424C= ENSP00000495146.2:p.Ser1475=
ENST00000642365.2:c.4574C= ENSP00000495459.2:p.Ser1525=
ENST00000644417.2:c.*4957C= ENSP00000493912.2:n.*4957C=
ENST00000646464.2:c.*7326C= ENSP00000496610.2:n.*7326C=
ENST00000219476.9:c.4577C= MANE Select ENSP00000219476.3:p.Ser1526=
ENST00000350773.9:c.4508C= ENSP00000344383.4:p.Ser1503=
ENST00000401874.7:c.4376C= ENSP00000384468.2:p.Ser1459=
ENST00000568454.6:c.4409C= ENSP00000454487.1:p.Ser1470=
ENST00000569110.2:c.800C=
ENST00000569930.2:n.2459C=
ENST00000642365.1:c.3231C=
ENST00000642561.1:c.4448C= ENSP00000495099.1:p.Ser1483=
ENST00000642728.1:n.759C=
ENST00000642791.1:n.174C=
ENST00000642797.1:c.4379C= ENSP00000493846.1:p.Ser1460=
ENST00000642936.1:c.4445C= ENSP00000494514.1:p.Ser1482=
ENST00000643088.1:c.4370C= ENSP00000494747.1:p.Ser1457=
ENST00000643177.1:n.591C=
ENST00000643426.1:n.2225C=
ENST00000643946.1:c.4502C= ENSP00000495927.1:p.Ser1501=
ENST00000644043.1:c.4448C= ENSP00000496262.1:p.Ser1483=
ENST00000644278.1:n.59C=
ENST00000644329.1:c.4376C= ENSP00000496611.1:p.Ser1459=
ENST00000644335.1:c.4373C= ENSP00000496317.1:p.Ser1458=
ENST00000644399.1:c.4498C=
ENST00000645024.1:n.2661C=
ENST00000646388.1:c.4571C= ENSP00000495921.1:p.Ser1524=
ENST00000646634.1:n.3392C=
ENST00000646674.1:n.1829C=
ENST00000647042.1:n.1800C=
ENST00000647180.1:n.1690C=
ENST00000219476.7:c.4577C= ENSP00000219476.3:p.Ser1526=
ENST00000350773.8:c.4508C= ENSP00000344383.4:p.Ser1503=
ENST00000382538.10:c.4232C= ENSP00000371978.6:p.Ser1411=
ENST00000401874.6:c.4376C= ENSP00000384468.2:p.Ser1459=
ENST00000439117.6:c.*3744C= ENSP00000406980.2:n.*3744C=
ENST00000439673.6:c.4268C= ENSP00000399232.2:p.Ser1423=
ENST00000497886.5:n.2335C=
ENST00000568454.5:c.4409C= ENSP00000454487.1:p.Ser1470=
ENST00000569110.1:c.759C=
ENST00000569930.1:n.1692C=
NM_000548.3:c.4577C= , LRG_487t1:c.4577C= NP_000539.2:p.Ser1526=
NM_001077183.1:c.4376C= NP_001070651.1:p.Ser1459=
NM_001114382.1:c.4508C= NP_001107854.1:p.Ser1503=
XM_005255529.3:c.4448C= XP_005255586.2:p.Ser1483=
XM_005255531.3:c.4379C= XP_005255588.2:p.Ser1460=
XM_011522636.1:c.4631C= XP_011520938.1:p.Ser1544=
XM_011522637.1:c.4628C= XP_011520939.1:p.Ser1543=
XM_011522638.1:c.4520C= XP_011520940.1:p.Ser1507=
XM_011522639.1:c.4502C= XP_011520941.1:p.Ser1501=
XM_011522640.1:c.4499C= XP_011520942.1:p.Ser1500=
XM_011522641.1:c.4268C= XP_011520943.1:p.Ser1423=
NM_000548.4:c.4577C= NP_000539.2:p.Ser1526=
NM_001077183.2:c.4376C= NP_001070651.1:p.Ser1459=
NM_001114382.2:c.4508C= NP_001107854.1:p.Ser1503=
NM_001318827.1:c.4268C= NP_001305756.1:p.Ser1423=
NM_001318829.1:c.4232C= NP_001305758.1:p.Ser1411=
NM_001318831.1:c.3845C= NP_001305760.1:p.Ser1282=
NM_001318832.1:c.4409C= NP_001305761.1:p.Ser1470=
NM_001363528.1:c.4379C= NP_001350457.1:p.Ser1460=
NM_021055.2:c.4448C= NP_066399.2:p.Ser1483=
XM_005255531.4:c.4379C= XP_005255588.2:p.Ser1460=
XM_011522636.2:c.4631C= XP_011520938.1:p.Ser1544=
XM_011522637.2:c.4628C= XP_011520939.1:p.Ser1543=
XM_011522638.2:c.4793C= XP_011520940.2:p.Ser1598=
XM_011522639.2:c.4502C= XP_011520941.1:p.Ser1501=
XM_011522640.2:c.4499C= XP_011520942.1:p.Ser1500=
XM_017023615.1:c.4574C= XP_016879104.1:p.Ser1525=
XM_017023616.1:c.4445C= XP_016879105.1:p.Ser1482=
XM_017023617.1:c.4541C= XP_016879106.1:p.Ser1514=
XM_017023618.1:c.3287C= XP_016879107.1:p.Ser1096=
XM_024450413.1:c.4376C= XP_024306181.1:p.Ser1459=
NM_000548.5:c.4577C= MANE Select NP_000539.2:p.Ser1526=
NM_001370404.1:c.4445C= NP_001357333.1:p.Ser1482=
NM_001370405.1:c.4448C= NP_001357334.1:p.Ser1483=
NM_001077183.3:c.4376C= NP_001070651.1:p.Ser1459=
NM_001114382.3:c.4508C= NP_001107854.1:p.Ser1503=
NM_001318827.2:c.4268C= NP_001305756.1:p.Ser1423=
NM_001318829.2:c.4232C= NP_001305758.1:p.Ser1411=
NM_001318831.2:c.3845C= NP_001305760.1:p.Ser1282=
NM_001318832.2:c.4409C= NP_001305761.1:p.Ser1470=
NM_001363528.2:c.4379C= NP_001350457.1:p.Ser1460=
NM_021055.3:c.4448C= NP_066399.2:p.Ser1483=