Canonical Allele Identifier: CA2201991477
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2048749_2048753delinsTGAGA , CM000678.2:g.2048749_2048753delinsTGAGA GRCh38
NC_000016.9:g.2098750_2098754delinsTGAGA , CM000678.1:g.2098750_2098754delinsTGAGA GRCh37
NC_000016.8:g.2038751_2038755delinsTGAGA NCBI36
NG_005895.1:g.4444_4448delinsTGAGA , LRG_487:g.4444_4448delinsTGAGA
NG_008412.1:g.4114_4118delinsTCTCA

Transcript Alleles

HGVS Amino-acid change
ENST00000568566.6:c.134_138delinsTGAGA ENSP00000455997.2:p.Leu45=
ENST00000642206.2:c.134_138delinsTGAGA ENSP00000495146.2:p.Leu45=
ENST00000642365.2:c.134_138delinsTGAGA ENSP00000495459.2:p.Leu45=
ENST00000644417.2:c.134_138delinsTGAGA ENSP00000493912.2:p.Leu45=
ENST00000646464.2:c.134_138delinsTGAGA ENSP00000496610.2:p.Leu45=
ENST00000219476.9:c.134_138delinsTGAGA MANE Select ENSP00000219476.3:p.Leu45=
ENST00000350773.9:c.134_138delinsTGAGA ENSP00000344383.4:p.Leu45=
ENST00000401874.7:c.134_138delinsTGAGA ENSP00000384468.2:p.Leu45=
ENST00000461648.3:n.244_248delinsTGAGA
ENST00000568454.6:c.167_171delinsTGAGA ENSP00000454487.1:p.Leu56=
ENST00000568692.2:n.14_18delinsTGAGA
ENST00000642206.1:c.134_138delinsTGAGA ENSP00000495146.1:p.Leu45=
ENST00000642561.1:c.134_138delinsTGAGA ENSP00000495099.1:p.Leu45=
ENST00000642797.1:c.134_138delinsTGAGA ENSP00000493846.1:p.Leu45=
ENST00000642812.1:n.191_195delinsTGAGA
ENST00000642936.1:c.134_138delinsTGAGA ENSP00000494514.1:p.Leu45=
ENST00000643088.1:c.134_138delinsTGAGA ENSP00000494747.1:p.Leu45=
ENST00000643149.1:n.244_248delinsTGAGA
ENST00000643298.1:c.134_138delinsTGAGA ENSP00000494393.1:p.Leu45=
ENST00000643745.1:c.134_138delinsTGAGA ENSP00000495948.1:p.Leu45=
ENST00000643946.1:c.134_138delinsTGAGA ENSP00000495927.1:p.Leu45=
ENST00000644043.1:c.134_138delinsTGAGA ENSP00000496262.1:p.Leu45=
ENST00000644135.1:c.134_138delinsTGAGA ENSP00000495644.1:p.Leu45=
ENST00000644222.1:n.221_225delinsTGAGA
ENST00000644329.1:c.134_138delinsTGAGA ENSP00000496611.1:p.Leu45=
ENST00000644335.1:c.134_138delinsTGAGA ENSP00000496317.1:p.Leu45=
ENST00000644399.1:c.127_131delinsTGAGA
ENST00000644665.1:n.251_255delinsTGAGA
ENST00000645591.1:n.262_266delinsTGAGA
ENST00000646388.1:c.134_138delinsTGAGA ENSP00000495921.1:p.Leu45=
ENST00000647234.1:n.9_13delinsTGAGA
ENST00000219476.7:c.134_138delinsTGAGA ENSP00000219476.3:p.Leu45=
ENST00000350773.8:c.134_138delinsTGAGA ENSP00000344383.4:p.Leu45=
ENST00000382538.10:c.-10+684_-10+688delinsTGAGA ENSP00000371978.6:n.-10+684_-10+688delins...
ENST00000401874.6:c.134_138delinsTGAGA ENSP00000384468.2:p.Leu45=
ENST00000439117.6:c.134_138delinsTGAGA ENSP00000406980.2:p.Leu45=
ENST00000439673.6:c.134_138delinsTGAGA ENSP00000399232.2:p.Leu45=
ENST00000461648.2:n.239_243delinsTGAGA
ENST00000568454.5:c.167_171delinsTGAGA ENSP00000454487.1:p.Leu56=
NM_000548.3:c.134_138delinsTGAGA , LRG_487t1:c.134_138delinsTGAGA NP_000539.2:p.Leu45=
NM_001077183.1:c.134_138delinsTGAGA NP_001070651.1:p.Leu45=
NM_001114382.1:c.134_138delinsTGAGA NP_001107854.1:p.Leu45=
XM_005255529.3:c.134_138delinsTGAGA XP_005255586.2:p.Leu45=
XM_005255531.3:c.134_138delinsTGAGA XP_005255588.2:p.Leu45=
XM_011522636.1:c.134_138delinsTGAGA XP_011520938.1:p.Leu45=
XM_011522637.1:c.134_138delinsTGAGA XP_011520939.1:p.Leu45=
XM_011522638.1:c.134_138delinsTGAGA XP_011520940.1:p.Leu45=
XM_011522639.1:c.134_138delinsTGAGA XP_011520941.1:p.Leu45=
XM_011522640.1:c.134_138delinsTGAGA XP_011520942.1:p.Leu45=
XM_011522641.1:c.134_138delinsTGAGA XP_011520943.1:p.Leu45=
NM_000548.4:c.134_138delinsTGAGA NP_000539.2:p.Leu45=
NM_001077183.2:c.134_138delinsTGAGA NP_001070651.1:p.Leu45=
NM_001114382.2:c.134_138delinsTGAGA NP_001107854.1:p.Leu45=
NM_001318827.1:c.134_138delinsTGAGA NP_001305756.1:p.Leu45=
NM_001318829.1:c.-10+684_-10+688delinsTGAGA NP_001305758.1:n.-10+684_-10+688delinsTGA...
NM_001318831.1:c.-93_-89delinsTGAGA NP_001305760.1:n.-93_-89delinsTGAGA
NM_001318832.1:c.167_171delinsTGAGA NP_001305761.1:p.Leu56=
NM_001363528.1:c.134_138delinsTGAGA NP_001350457.1:p.Leu45=
NM_021055.2:c.134_138delinsTGAGA NP_066399.2:p.Leu45=
XM_005255531.4:c.134_138delinsTGAGA XP_005255588.2:p.Leu45=
XM_011522636.2:c.134_138delinsTGAGA XP_011520938.1:p.Leu45=
XM_011522637.2:c.134_138delinsTGAGA XP_011520939.1:p.Leu45=
XM_011522638.2:c.407_411delinsTGAGA XP_011520940.2:p.Leu136=
XM_011522639.2:c.134_138delinsTGAGA XP_011520941.1:p.Leu45=
XM_011522640.2:c.134_138delinsTGAGA XP_011520942.1:p.Leu45=
XM_017023615.1:c.134_138delinsTGAGA XP_016879104.1:p.Leu45=
XM_017023616.1:c.134_138delinsTGAGA XP_016879105.1:p.Leu45=
XM_017023617.1:c.407_411delinsTGAGA XP_016879106.1:p.Leu136=
XM_017023618.1:c.-1298_-1294delinsTGAGA XP_016879107.1:n.-1298_-1294delinsTGAGA
XM_024450413.1:c.134_138delinsTGAGA XP_024306181.1:p.Leu45=
NM_000548.5:c.134_138delinsTGAGA MANE Select NP_000539.2:p.Leu45=
NM_001370404.1:c.134_138delinsTGAGA NP_001357333.1:p.Leu45=
NM_001370405.1:c.134_138delinsTGAGA NP_001357334.1:p.Leu45=
NM_001077183.3:c.134_138delinsTGAGA NP_001070651.1:p.Leu45=
NM_001114382.3:c.134_138delinsTGAGA NP_001107854.1:p.Leu45=
NM_001318827.2:c.134_138delinsTGAGA NP_001305756.1:p.Leu45=
NM_001318829.2:c.-10+684_-10+688delinsTGAGA NP_001305758.1:n.-10+684_-10+688delinsTGA...
NM_001318831.2:c.-93_-89delinsTGAGA NP_001305760.1:n.-93_-89delinsTGAGA
NM_001318832.2:c.167_171delinsTGAGA NP_001305761.1:p.Leu56=
NM_001363528.2:c.134_138delinsTGAGA NP_001350457.1:p.Leu45=
NM_021055.3:c.134_138delinsTGAGA NP_066399.2:p.Leu45=