Canonical Allele Identifier: CA2202044445
Community Standard Title: NM_000548.5(TSC2):c.4227G= (p.Arg1409=)
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2084449G= , CM000678.2:g.2084449G= GRCh38
NC_000016.9:g.2134450G= , CM000678.1:g.2134450G= GRCh37
NC_000016.8:g.2074451G= NCBI36
NG_005895.1:g.40144G= , LRG_487:g.40144G=

Transcript Alleles

HGVS Amino-acid Change
NM_000548.5:c.4227G= MANE Select NP_000539.2:p.Arg1409=
ENST00000219476.9:c.4227G= MANE Select ENSP00000219476.3:p.Arg1409=
NM_000548.3:c.4227G= , LRG_487t1:c.4227G= NP_000539.2:p.Arg1409=
NM_000548.4:c.4227G= NP_000539.2:p.Arg1409=
NM_001077183.1:c.4026G= NP_001070651.1:p.Arg1342=
NM_001077183.2:c.4026G= NP_001070651.1:p.Arg1342=
NM_001077183.3:c.4026G= NP_001070651.1:p.Arg1342=
NM_001114382.1:c.4158G= NP_001107854.1:p.Arg1386=
NM_001114382.2:c.4158G= NP_001107854.1:p.Arg1386=
NM_001114382.3:c.4158G= NP_001107854.1:p.Arg1386=
NM_001318827.1:c.3918G= NP_001305756.1:p.Arg1306=
NM_001318827.2:c.3918G= NP_001305756.1:p.Arg1306=
NM_001318829.1:c.3882G= NP_001305758.1:p.Arg1294=
NM_001318829.2:c.3882G= NP_001305758.1:p.Arg1294=
NM_001318831.1:c.3495G= NP_001305760.1:p.Arg1165=
NM_001318831.2:c.3495G= NP_001305760.1:p.Arg1165=
NM_001318832.1:c.4059G= NP_001305761.1:p.Arg1353=
NM_001318832.2:c.4059G= NP_001305761.1:p.Arg1353=
NM_001363528.1:c.4029G= NP_001350457.1:p.Arg1343=
NM_001363528.2:c.4029G= NP_001350457.1:p.Arg1343=
NM_001370404.1:c.4095G= NP_001357333.1:p.Arg1365=
NM_001370405.1:c.4098G= NP_001357334.1:p.Arg1366=
NM_021055.2:c.4098G= NP_066399.2:p.Arg1366=
NM_021055.3:c.4098G= NP_066399.2:p.Arg1366=
ENST00000219476.7:c.4227G= ENSP00000219476.3:p.Arg1409=
ENST00000350773.8:c.4158G= ENSP00000344383.4:p.Arg1386=
ENST00000350773.9:c.4158G= ENSP00000344383.4:p.Arg1386=
ENST00000382538.10:c.3882G= ENSP00000371978.6:p.Arg1294=
ENST00000401874.6:c.4026G= ENSP00000384468.2:p.Arg1342=
ENST00000401874.7:c.4026G= ENSP00000384468.2:p.Arg1342=
ENST00000439117.6:c.*3394G= ENSP00000406980.2:n.*3394G=
ENST00000439673.6:c.3918G= ENSP00000399232.2:p.Arg1306=
ENST00000497886.5:n.1985G=
ENST00000568454.5:c.4059G= ENSP00000454487.1:p.Arg1353=
ENST00000568454.6:c.4059G= ENSP00000454487.1:p.Arg1353=
ENST00000568566.6:c.*2576G= ENSP00000455997.2:n.*2576G=
ENST00000569110.1:c.409G=
ENST00000569110.2:c.463G=
ENST00000569930.1:n.1342G=
ENST00000569930.2:n.2109G=
ENST00000642206.2:c.4074G= ENSP00000495146.2:p.Arg1358=
ENST00000642365.1:c.2881G=
ENST00000642365.2:c.4224G= ENSP00000495459.2:p.Arg1408=
ENST00000642561.1:c.4098G= ENSP00000495099.1:p.Arg1366=
ENST00000642728.1:n.409G=
ENST00000642797.1:c.4029G= ENSP00000493846.1:p.Arg1343=
ENST00000642936.1:c.4095G= ENSP00000494514.1:p.Arg1365=
ENST00000643088.1:c.4026G= ENSP00000494747.1:p.Arg1342=
ENST00000643177.1:n.241G=
ENST00000643426.1:n.1875G=
ENST00000643946.1:c.4158G= ENSP00000495927.1:p.Arg1386=
ENST00000644043.1:c.4098G= ENSP00000496262.1:p.Arg1366=
ENST00000644329.1:c.4026G= ENSP00000496611.1:p.Arg1342=
ENST00000644335.1:c.4029G= ENSP00000496317.1:p.Arg1343=
ENST00000644399.1:c.4148G=
ENST00000644417.2:c.*4607G= ENSP00000493912.2:n.*4607G=
ENST00000645024.1:n.2311G=
ENST00000645186.1:c.470G=
ENST00000646388.1:c.4227G= ENSP00000495921.1:p.Arg1409=
ENST00000646464.2:c.*6976G= ENSP00000496610.2:n.*6976G=
ENST00000646634.1:n.3042G=
ENST00000646674.1:n.1479G=
ENST00000647042.1:n.1450G=
ENST00000647180.1:n.1340G=
XM_005255529.3:c.4098G= XP_005255586.2:p.Arg1366=
XM_005255531.3:c.4029G= XP_005255588.2:p.Arg1343=
XM_005255531.4:c.4029G= XP_005255588.2:p.Arg1343=
XM_011522636.1:c.4281G= XP_011520938.1:p.Arg1427=
XM_011522636.2:c.4281G= XP_011520938.1:p.Arg1427=
XM_011522637.1:c.4278G= XP_011520939.1:p.Arg1426=
XM_011522637.2:c.4278G= XP_011520939.1:p.Arg1426=
XM_011522638.1:c.4170G= XP_011520940.1:p.Arg1390=
XM_011522638.2:c.4443G= XP_011520940.2:p.Arg1481=
XM_011522639.1:c.4152G= XP_011520941.1:p.Arg1384=
XM_011522639.2:c.4152G= XP_011520941.1:p.Arg1384=
XM_011522640.1:c.4149G= XP_011520942.1:p.Arg1383=
XM_011522640.2:c.4149G= XP_011520942.1:p.Arg1383=
XM_011522641.1:c.3918G= XP_011520943.1:p.Arg1306=
XM_017023615.1:c.4224G= XP_016879104.1:p.Arg1408=
XM_017023616.1:c.4095G= XP_016879105.1:p.Arg1365=
XM_017023617.1:c.4191G= XP_016879106.1:p.Arg1397=
XM_017023618.1:c.2937G= XP_016879107.1:p.Arg979=
XM_024450413.1:c.4026G= XP_024306181.1:p.Arg1342=