Canonical Allele Identifier: CA394314053
Gene: TSC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2088243A>G , CM000678.2:g.2088243A>G GRCh38
NC_000016.9:g.2138244A>G , CM000678.1:g.2138244A>G GRCh37
NC_000016.8:g.2078245A>G NCBI36
NG_005895.1:g.43938A>G , LRG_487:g.43938A>G
NG_008617.1:g.54978T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*3526A>G ENSP00000455997.2:n.*3526A>G
ENST00000642206.2:c.5024A>G ENSP00000495146.2:p.His1675Arg
ENST00000642365.2:c.5174A>G ENSP00000495459.2:p.His1725Arg
ENST00000644417.2:c.*5690A>G ENSP00000493912.2:n.*5690A>G
ENST00000646464.2:c.*7926A>G ENSP00000496610.2:n.*7926A>G
ENST00000219476.9:c.5177A>G MANE Select ENSP00000219476.3:p.His1726Arg
ENST00000350773.9:c.5108A>G ENSP00000344383.4:p.His1703Arg
ENST00000401874.7:c.4976A>G ENSP00000384468.2:p.His1659Arg
ENST00000568454.6:c.5009A>G ENSP00000454487.1:p.His1670Arg
ENST00000569110.2:c.1400A>G
ENST00000569930.2:n.3059A>G
ENST00000642365.1:c.3831A>G
ENST00000642561.1:c.5036A>G ENSP00000495099.1:p.His1679Arg
ENST00000642791.1:n.774A>G
ENST00000642797.1:c.4979A>G ENSP00000493846.1:p.His1660Arg
ENST00000642936.1:c.5045A>G ENSP00000494514.1:p.His1682Arg
ENST00000643088.1:c.4970A>G ENSP00000494747.1:p.His1657Arg
ENST00000643426.1:n.2825A>G
ENST00000643946.1:c.5102A>G ENSP00000495927.1:p.His1701Arg
ENST00000644043.1:c.5048A>G ENSP00000496262.1:p.His1683Arg
ENST00000644329.1:c.5063A>G ENSP00000496611.1:p.His1688Arg
ENST00000644335.1:c.4973A>G ENSP00000496317.1:p.His1658Arg
ENST00000644399.1:c.5098A>G
ENST00000645024.1:n.3261A>G
ENST00000646388.1:c.5171A>G ENSP00000495921.1:p.His1724Arg
ENST00000646634.1:n.3992A>G
ENST00000646674.1:n.2429A>G
ENST00000647042.1:n.2400A>G
ENST00000647180.1:n.2290A>G
ENST00000219476.7:c.5177A>G ENSP00000219476.3:p.His1726Arg
ENST00000350773.8:c.5108A>G ENSP00000344383.4:p.His1703Arg
ENST00000382538.10:c.4832A>G ENSP00000371978.6:p.His1611Arg
ENST00000401874.6:c.4976A>G ENSP00000384468.2:p.His1659Arg
ENST00000439117.6:c.*4344A>G ENSP00000406980.2:n.*4344A>G
ENST00000439673.6:c.4868A>G ENSP00000399232.2:p.His1623Arg
ENST00000497886.5:n.2900A>G
ENST00000568454.5:c.5009A>G ENSP00000454487.1:p.His1670Arg
ENST00000569110.1:c.1359A>G
ENST00000569930.1:n.2292A>G
NM_000548.3:c.5177A>G , LRG_487t1:c.5177A>G NP_000539.2:p.His1726Arg
NM_001077183.1:c.4976A>G NP_001070651.1:p.His1659Arg
NM_001114382.1:c.5108A>G NP_001107854.1:p.His1703Arg
XM_005255529.3:c.5048A>G XP_005255586.2:p.His1683Arg
XM_005255531.3:c.4979A>G XP_005255588.2:p.His1660Arg
XM_011522636.1:c.5231A>G XP_011520938.1:p.His1744Arg
XM_011522637.1:c.5228A>G XP_011520939.1:p.His1743Arg
XM_011522638.1:c.5120A>G XP_011520940.1:p.His1707Arg
XM_011522639.1:c.5102A>G XP_011520941.1:p.His1701Arg
XM_011522640.1:c.5099A>G XP_011520942.1:p.His1700Arg
XM_011522641.1:c.4868A>G XP_011520943.1:p.His1623Arg
NM_000548.4:c.5177A>G NP_000539.2:p.His1726Arg
NM_001077183.2:c.4976A>G NP_001070651.1:p.His1659Arg
NM_001114382.2:c.5108A>G NP_001107854.1:p.His1703Arg
NM_001318827.1:c.4868A>G NP_001305756.1:p.His1623Arg
NM_001318829.1:c.4832A>G NP_001305758.1:p.His1611Arg
NM_001318831.1:c.4445A>G NP_001305760.1:p.His1482Arg
NM_001318832.1:c.5009A>G NP_001305761.1:p.His1670Arg
NM_001363528.1:c.4979A>G NP_001350457.1:p.His1660Arg
NM_021055.2:c.5048A>G NP_066399.2:p.His1683Arg
XM_005255531.4:c.4979A>G XP_005255588.2:p.His1660Arg
XM_011522636.2:c.5231A>G XP_011520938.1:p.His1744Arg
XM_011522637.2:c.5228A>G XP_011520939.1:p.His1743Arg
XM_011522638.2:c.5393A>G XP_011520940.2:p.His1798Arg
XM_011522639.2:c.5102A>G XP_011520941.1:p.His1701Arg
XM_011522640.2:c.5099A>G XP_011520942.1:p.His1700Arg
XM_017023615.1:c.5174A>G XP_016879104.1:p.His1725Arg
XM_017023616.1:c.5045A>G XP_016879105.1:p.His1682Arg
XM_017023617.1:c.5141A>G XP_016879106.1:p.His1714Arg
XM_017023618.1:c.3887A>G XP_016879107.1:p.His1296Arg
XM_024450413.1:c.5063A>G XP_024306181.1:p.His1688Arg
NM_000548.5:c.5177A>G MANE Select NP_000539.2:p.His1726Arg
NM_001370404.1:c.5045A>G NP_001357333.1:p.His1682Arg
NM_001370405.1:c.5036A>G NP_001357334.1:p.His1679Arg
NM_001077183.3:c.4976A>G NP_001070651.1:p.His1659Arg
NM_001114382.3:c.5108A>G NP_001107854.1:p.His1703Arg
NM_001318827.2:c.4868A>G NP_001305756.1:p.His1623Arg
NM_001318829.2:c.4832A>G NP_001305758.1:p.His1611Arg
NM_001318831.2:c.4445A>G NP_001305760.1:p.His1482Arg
NM_001318832.2:c.5009A>G NP_001305761.1:p.His1670Arg
NM_001363528.2:c.4979A>G NP_001350457.1:p.His1660Arg
NM_021055.3:c.5048A>G NP_066399.2:p.His1683Arg