Canonical Allele Identifier: CA2202019486
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2085293A= , CM000678.2:g.2085293A= GRCh38
NC_000016.9:g.2135294A= , CM000678.1:g.2135294A= GRCh37
NC_000016.8:g.2075295A= NCBI36
NG_005895.1:g.40988A= , LRG_487:g.40988A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*2982A= ENSP00000455997.2:n.*2982A=
ENST00000642206.2:c.4480A= ENSP00000495146.2:p.Ile1494=
ENST00000642365.2:c.4630A= ENSP00000495459.2:p.Ile1544=
ENST00000644417.2:c.*5013A= ENSP00000493912.2:n.*5013A=
ENST00000646464.2:c.*7382A= ENSP00000496610.2:n.*7382A=
ENST00000219476.9:c.4633A= MANE Select ENSP00000219476.3:p.Ile1545=
ENST00000350773.9:c.4564A= ENSP00000344383.4:p.Ile1522=
ENST00000401874.7:c.4432A= ENSP00000384468.2:p.Ile1478=
ENST00000568454.6:c.4465A= ENSP00000454487.1:p.Ile1489=
ENST00000569110.2:c.856A=
ENST00000569930.2:n.2515A=
ENST00000642365.1:c.3287A=
ENST00000642561.1:c.4504A= ENSP00000495099.1:p.Ile1502=
ENST00000642728.1:n.815A=
ENST00000642791.1:n.230A=
ENST00000642797.1:c.4435A= ENSP00000493846.1:p.Ile1479=
ENST00000642936.1:c.4501A= ENSP00000494514.1:p.Ile1501=
ENST00000643088.1:c.4426A= ENSP00000494747.1:p.Ile1476=
ENST00000643177.1:n.647A=
ENST00000643426.1:n.2281A=
ENST00000643946.1:c.4558A= ENSP00000495927.1:p.Ile1520=
ENST00000644043.1:c.4504A= ENSP00000496262.1:p.Ile1502=
ENST00000644278.1:n.115A=
ENST00000644329.1:c.4432A= ENSP00000496611.1:p.Ile1478=
ENST00000644335.1:c.4429A= ENSP00000496317.1:p.Ile1477=
ENST00000644399.1:c.4554A=
ENST00000645024.1:n.2717A=
ENST00000646388.1:c.4627A= ENSP00000495921.1:p.Ile1543=
ENST00000646634.1:n.3448A=
ENST00000646674.1:n.1885A=
ENST00000647042.1:n.1856A=
ENST00000647180.1:n.1746A=
ENST00000219476.7:c.4633A= ENSP00000219476.3:p.Ile1545=
ENST00000350773.8:c.4564A= ENSP00000344383.4:p.Ile1522=
ENST00000382538.10:c.4288A= ENSP00000371978.6:p.Ile1430=
ENST00000401874.6:c.4432A= ENSP00000384468.2:p.Ile1478=
ENST00000439117.6:c.*3800A= ENSP00000406980.2:n.*3800A=
ENST00000439673.6:c.4324A= ENSP00000399232.2:p.Ile1442=
ENST00000497886.5:n.2391A=
ENST00000568454.5:c.4465A= ENSP00000454487.1:p.Ile1489=
ENST00000569110.1:c.815A=
ENST00000569930.1:n.1748A=
NM_000548.3:c.4633A= , LRG_487t1:c.4633A= NP_000539.2:p.Ile1545=
NM_001077183.1:c.4432A= NP_001070651.1:p.Ile1478=
NM_001114382.1:c.4564A= NP_001107854.1:p.Ile1522=
XM_005255529.3:c.4504A= XP_005255586.2:p.Ile1502=
XM_005255531.3:c.4435A= XP_005255588.2:p.Ile1479=
XM_011522636.1:c.4687A= XP_011520938.1:p.Ile1563=
XM_011522637.1:c.4684A= XP_011520939.1:p.Ile1562=
XM_011522638.1:c.4576A= XP_011520940.1:p.Ile1526=
XM_011522639.1:c.4558A= XP_011520941.1:p.Ile1520=
XM_011522640.1:c.4555A= XP_011520942.1:p.Ile1519=
XM_011522641.1:c.4324A= XP_011520943.1:p.Ile1442=
NM_000548.4:c.4633A= NP_000539.2:p.Ile1545=
NM_001077183.2:c.4432A= NP_001070651.1:p.Ile1478=
NM_001114382.2:c.4564A= NP_001107854.1:p.Ile1522=
NM_001318827.1:c.4324A= NP_001305756.1:p.Ile1442=
NM_001318829.1:c.4288A= NP_001305758.1:p.Ile1430=
NM_001318831.1:c.3901A= NP_001305760.1:p.Ile1301=
NM_001318832.1:c.4465A= NP_001305761.1:p.Ile1489=
NM_001363528.1:c.4435A= NP_001350457.1:p.Ile1479=
NM_021055.2:c.4504A= NP_066399.2:p.Ile1502=
XM_005255531.4:c.4435A= XP_005255588.2:p.Ile1479=
XM_011522636.2:c.4687A= XP_011520938.1:p.Ile1563=
XM_011522637.2:c.4684A= XP_011520939.1:p.Ile1562=
XM_011522638.2:c.4849A= XP_011520940.2:p.Ile1617=
XM_011522639.2:c.4558A= XP_011520941.1:p.Ile1520=
XM_011522640.2:c.4555A= XP_011520942.1:p.Ile1519=
XM_017023615.1:c.4630A= XP_016879104.1:p.Ile1544=
XM_017023616.1:c.4501A= XP_016879105.1:p.Ile1501=
XM_017023617.1:c.4597A= XP_016879106.1:p.Ile1533=
XM_017023618.1:c.3343A= XP_016879107.1:p.Ile1115=
XM_024450413.1:c.4432A= XP_024306181.1:p.Ile1478=
NM_000548.5:c.4633A= MANE Select NP_000539.2:p.Ile1545=
NM_001370404.1:c.4501A= NP_001357333.1:p.Ile1501=
NM_001370405.1:c.4504A= NP_001357334.1:p.Ile1502=
NM_001077183.3:c.4432A= NP_001070651.1:p.Ile1478=
NM_001114382.3:c.4564A= NP_001107854.1:p.Ile1522=
NM_001318827.2:c.4324A= NP_001305756.1:p.Ile1442=
NM_001318829.2:c.4288A= NP_001305758.1:p.Ile1430=
NM_001318831.2:c.3901A= NP_001305760.1:p.Ile1301=
NM_001318832.2:c.4465A= NP_001305761.1:p.Ile1489=
NM_001363528.2:c.4435A= NP_001350457.1:p.Ile1479=
NM_021055.3:c.4504A= NP_066399.2:p.Ile1502=