Canonical Allele Identifier: CA2202018290
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2085013T= , CM000678.2:g.2085013T= GRCh38
NC_000016.9:g.2135014T= , CM000678.1:g.2135014T= GRCh37
NC_000016.8:g.2075015T= NCBI36
NG_005895.1:g.40708T= , LRG_487:g.40708T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*2905T= ENSP00000455997.2:n.*2905T=
ENST00000642206.2:c.4403T= ENSP00000495146.2:p.Leu1468=
ENST00000642365.2:c.4553T= ENSP00000495459.2:p.Leu1518=
ENST00000644417.2:c.*4936T= ENSP00000493912.2:n.*4936T=
ENST00000646464.2:c.*7305T= ENSP00000496610.2:n.*7305T=
ENST00000219476.9:c.4556T= MANE Select ENSP00000219476.3:p.Leu1519=
ENST00000350773.9:c.4487T= ENSP00000344383.4:p.Leu1496=
ENST00000401874.7:c.4355T= ENSP00000384468.2:p.Leu1452=
ENST00000568454.6:c.4388T= ENSP00000454487.1:p.Leu1463=
ENST00000569110.2:c.779T=
ENST00000569930.2:n.2438T=
ENST00000642365.1:c.3210T=
ENST00000642561.1:c.4427T= ENSP00000495099.1:p.Leu1476=
ENST00000642728.1:n.738T=
ENST00000642797.1:c.4358T= ENSP00000493846.1:p.Leu1453=
ENST00000642936.1:c.4424T= ENSP00000494514.1:p.Leu1475=
ENST00000643088.1:c.4355T= ENSP00000494747.1:p.Leu1452=
ENST00000643177.1:n.570T=
ENST00000643426.1:n.2204T=
ENST00000643946.1:c.4487T= ENSP00000495927.1:p.Leu1496=
ENST00000644043.1:c.4427T= ENSP00000496262.1:p.Leu1476=
ENST00000644329.1:c.4355T= ENSP00000496611.1:p.Leu1452=
ENST00000644335.1:c.4358T= ENSP00000496317.1:p.Leu1453=
ENST00000644399.1:c.4477T=
ENST00000645024.1:n.2640T=
ENST00000646388.1:c.4556T= ENSP00000495921.1:p.Leu1519=
ENST00000646634.1:n.3371T=
ENST00000646674.1:n.1808T=
ENST00000647042.1:n.1779T=
ENST00000647180.1:n.1669T=
ENST00000219476.7:c.4556T= ENSP00000219476.3:p.Leu1519=
ENST00000350773.8:c.4487T= ENSP00000344383.4:p.Leu1496=
ENST00000382538.10:c.4211T= ENSP00000371978.6:p.Leu1404=
ENST00000401874.6:c.4355T= ENSP00000384468.2:p.Leu1452=
ENST00000439117.6:c.*3723T= ENSP00000406980.2:n.*3723T=
ENST00000439673.6:c.4247T= ENSP00000399232.2:p.Leu1416=
ENST00000497886.5:n.2314T=
ENST00000568454.5:c.4388T= ENSP00000454487.1:p.Leu1463=
ENST00000569110.1:c.738T=
ENST00000569930.1:n.1671T=
NM_000548.3:c.4556T= , LRG_487t1:c.4556T= NP_000539.2:p.Leu1519=
NM_001077183.1:c.4355T= NP_001070651.1:p.Leu1452=
NM_001114382.1:c.4487T= NP_001107854.1:p.Leu1496=
XM_005255529.3:c.4427T= XP_005255586.2:p.Leu1476=
XM_005255531.3:c.4358T= XP_005255588.2:p.Leu1453=
XM_011522636.1:c.4610T= XP_011520938.1:p.Leu1537=
XM_011522637.1:c.4607T= XP_011520939.1:p.Leu1536=
XM_011522638.1:c.4499T= XP_011520940.1:p.Leu1500=
XM_011522639.1:c.4481T= XP_011520941.1:p.Leu1494=
XM_011522640.1:c.4478T= XP_011520942.1:p.Leu1493=
XM_011522641.1:c.4247T= XP_011520943.1:p.Leu1416=
NM_000548.4:c.4556T= NP_000539.2:p.Leu1519=
NM_001077183.2:c.4355T= NP_001070651.1:p.Leu1452=
NM_001114382.2:c.4487T= NP_001107854.1:p.Leu1496=
NM_001318827.1:c.4247T= NP_001305756.1:p.Leu1416=
NM_001318829.1:c.4211T= NP_001305758.1:p.Leu1404=
NM_001318831.1:c.3824T= NP_001305760.1:p.Leu1275=
NM_001318832.1:c.4388T= NP_001305761.1:p.Leu1463=
NM_001363528.1:c.4358T= NP_001350457.1:p.Leu1453=
NM_021055.2:c.4427T= NP_066399.2:p.Leu1476=
XM_005255531.4:c.4358T= XP_005255588.2:p.Leu1453=
XM_011522636.2:c.4610T= XP_011520938.1:p.Leu1537=
XM_011522637.2:c.4607T= XP_011520939.1:p.Leu1536=
XM_011522638.2:c.4772T= XP_011520940.2:p.Leu1591=
XM_011522639.2:c.4481T= XP_011520941.1:p.Leu1494=
XM_011522640.2:c.4478T= XP_011520942.1:p.Leu1493=
XM_017023615.1:c.4553T= XP_016879104.1:p.Leu1518=
XM_017023616.1:c.4424T= XP_016879105.1:p.Leu1475=
XM_017023617.1:c.4520T= XP_016879106.1:p.Leu1507=
XM_017023618.1:c.3266T= XP_016879107.1:p.Leu1089=
XM_024450413.1:c.4355T= XP_024306181.1:p.Leu1452=
NM_000548.5:c.4556T= MANE Select NP_000539.2:p.Leu1519=
NM_001370404.1:c.4424T= NP_001357333.1:p.Leu1475=
NM_001370405.1:c.4427T= NP_001357334.1:p.Leu1476=
NM_001077183.3:c.4355T= NP_001070651.1:p.Leu1452=
NM_001114382.3:c.4487T= NP_001107854.1:p.Leu1496=
NM_001318827.2:c.4247T= NP_001305756.1:p.Leu1416=
NM_001318829.2:c.4211T= NP_001305758.1:p.Leu1404=
NM_001318831.2:c.3824T= NP_001305760.1:p.Leu1275=
NM_001318832.2:c.4388T= NP_001305761.1:p.Leu1463=
NM_001363528.2:c.4358T= NP_001350457.1:p.Leu1453=
NM_021055.3:c.4427T= NP_066399.2:p.Leu1476=