Canonical Allele Identifier: CA2202031964
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2088268T= , CM000678.2:g.2088268T= GRCh38
NC_000016.9:g.2138269T= , CM000678.1:g.2138269T= GRCh37
NC_000016.8:g.2078270T= NCBI36
NG_005895.1:g.43963T= , LRG_487:g.43963T=
NG_008617.1:g.54953A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*3551T= ENSP00000455997.2:n.*3551T=
ENST00000642206.2:c.5049T= ENSP00000495146.2:p.Asp1683=
ENST00000642365.2:c.5199T= ENSP00000495459.2:p.Asp1733=
ENST00000644417.2:c.*5715T= ENSP00000493912.2:n.*5715T=
ENST00000646464.2:c.*7951T= ENSP00000496610.2:n.*7951T=
ENST00000219476.9:c.5202T= MANE Select ENSP00000219476.3:p.Asp1734=
ENST00000350773.9:c.5133T= ENSP00000344383.4:p.Asp1711=
ENST00000401874.7:c.5001T= ENSP00000384468.2:p.Asp1667=
ENST00000568454.6:c.5034T= ENSP00000454487.1:p.Asp1678=
ENST00000569110.2:c.1425T=
ENST00000569930.2:n.3084T=
ENST00000642365.1:c.3856T=
ENST00000642561.1:c.5061T= ENSP00000495099.1:p.Asp1687=
ENST00000642791.1:n.799T=
ENST00000642797.1:c.5004T= ENSP00000493846.1:p.Asp1668=
ENST00000642936.1:c.5070T= ENSP00000494514.1:p.Asp1690=
ENST00000643088.1:c.4995T= ENSP00000494747.1:p.Asp1665=
ENST00000643426.1:n.2850T=
ENST00000643946.1:c.5127T= ENSP00000495927.1:p.Asp1709=
ENST00000644043.1:c.5073T= ENSP00000496262.1:p.Asp1691=
ENST00000644329.1:c.5088T= ENSP00000496611.1:p.Asp1696=
ENST00000644335.1:c.4998T= ENSP00000496317.1:p.Asp1666=
ENST00000644399.1:c.5123T=
ENST00000645024.1:n.3286T=
ENST00000646388.1:c.5196T= ENSP00000495921.1:p.Asp1732=
ENST00000646634.1:n.4017T=
ENST00000646674.1:n.2454T=
ENST00000647042.1:n.2425T=
ENST00000647180.1:n.2315T=
ENST00000219476.7:c.5202T= ENSP00000219476.3:p.Asp1734=
ENST00000350773.8:c.5133T= ENSP00000344383.4:p.Asp1711=
ENST00000382538.10:c.4857T= ENSP00000371978.6:p.Asp1619=
ENST00000401874.6:c.5001T= ENSP00000384468.2:p.Asp1667=
ENST00000439117.6:c.*4369T= ENSP00000406980.2:n.*4369T=
ENST00000439673.6:c.4893T= ENSP00000399232.2:p.Asp1631=
ENST00000497886.5:n.2925T=
ENST00000568454.5:c.5034T= ENSP00000454487.1:p.Asp1678=
ENST00000569110.1:c.1384T=
ENST00000569930.1:n.2317T=
NM_000548.3:c.5202T= , LRG_487t1:c.5202T= NP_000539.2:p.Asp1734=
NM_001077183.1:c.5001T= NP_001070651.1:p.Asp1667=
NM_001114382.1:c.5133T= NP_001107854.1:p.Asp1711=
XM_005255529.3:c.5073T= XP_005255586.2:p.Asp1691=
XM_005255531.3:c.5004T= XP_005255588.2:p.Asp1668=
XM_011522636.1:c.5256T= XP_011520938.1:p.Asp1752=
XM_011522637.1:c.5253T= XP_011520939.1:p.Asp1751=
XM_011522638.1:c.5145T= XP_011520940.1:p.Asp1715=
XM_011522639.1:c.5127T= XP_011520941.1:p.Asp1709=
XM_011522640.1:c.5124T= XP_011520942.1:p.Asp1708=
XM_011522641.1:c.4893T= XP_011520943.1:p.Asp1631=
NM_000548.4:c.5202T= NP_000539.2:p.Asp1734=
NM_001077183.2:c.5001T= NP_001070651.1:p.Asp1667=
NM_001114382.2:c.5133T= NP_001107854.1:p.Asp1711=
NM_001318827.1:c.4893T= NP_001305756.1:p.Asp1631=
NM_001318829.1:c.4857T= NP_001305758.1:p.Asp1619=
NM_001318831.1:c.4470T= NP_001305760.1:p.Asp1490=
NM_001318832.1:c.5034T= NP_001305761.1:p.Asp1678=
NM_001363528.1:c.5004T= NP_001350457.1:p.Asp1668=
NM_021055.2:c.5073T= NP_066399.2:p.Asp1691=
XM_005255531.4:c.5004T= XP_005255588.2:p.Asp1668=
XM_011522636.2:c.5256T= XP_011520938.1:p.Asp1752=
XM_011522637.2:c.5253T= XP_011520939.1:p.Asp1751=
XM_011522638.2:c.5418T= XP_011520940.2:p.Asp1806=
XM_011522639.2:c.5127T= XP_011520941.1:p.Asp1709=
XM_011522640.2:c.5124T= XP_011520942.1:p.Asp1708=
XM_017023615.1:c.5199T= XP_016879104.1:p.Asp1733=
XM_017023616.1:c.5070T= XP_016879105.1:p.Asp1690=
XM_017023617.1:c.5166T= XP_016879106.1:p.Asp1722=
XM_017023618.1:c.3912T= XP_016879107.1:p.Asp1304=
XM_024450413.1:c.5088T= XP_024306181.1:p.Asp1696=
NM_000548.5:c.5202T= MANE Select NP_000539.2:p.Asp1734=
NM_001370404.1:c.5070T= NP_001357333.1:p.Asp1690=
NM_001370405.1:c.5061T= NP_001357334.1:p.Asp1687=
NM_001077183.3:c.5001T= NP_001070651.1:p.Asp1667=
NM_001114382.3:c.5133T= NP_001107854.1:p.Asp1711=
NM_001318827.2:c.4893T= NP_001305756.1:p.Asp1631=
NM_001318829.2:c.4857T= NP_001305758.1:p.Asp1619=
NM_001318831.2:c.4470T= NP_001305760.1:p.Asp1490=
NM_001318832.2:c.5034T= NP_001305761.1:p.Asp1678=
NM_001363528.2:c.5004T= NP_001350457.1:p.Asp1668=
NM_021055.3:c.5073T= NP_066399.2:p.Asp1691=