Canonical Allele Identifier: CA394297440
Community Standard Title: NM_000548.5(TSC2):c.3958G>T (p.Val1320Phe)
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2083769G>T , CM000678.2:g.2083769G>T GRCh38
NC_000016.9:g.2133770G>T , CM000678.1:g.2133770G>T GRCh37
NC_000016.8:g.2073771G>T NCBI36
NG_005895.1:g.39464G>T , LRG_487:g.39464G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000548.5:c.3958G>T MANE Select NP_000539.2:p.Val1320Phe
ENST00000219476.9:c.3958G>T MANE Select ENSP00000219476.3:p.Val1320Phe
NM_000548.3:c.3958G>T , LRG_487t1:c.3958G>T NP_000539.2:p.Val1320Phe
NM_000548.4:c.3958G>T NP_000539.2:p.Val1320Phe
NM_001077183.1:c.3757G>T NP_001070651.1:p.Val1253Phe
NM_001077183.2:c.3757G>T NP_001070651.1:p.Val1253Phe
NM_001077183.3:c.3757G>T NP_001070651.1:p.Val1253Phe
NM_001114382.1:c.3889G>T NP_001107854.1:p.Val1297Phe
NM_001114382.2:c.3889G>T NP_001107854.1:p.Val1297Phe
NM_001114382.3:c.3889G>T NP_001107854.1:p.Val1297Phe
NM_001318827.1:c.3649G>T NP_001305756.1:p.Val1217Phe
NM_001318827.2:c.3649G>T NP_001305756.1:p.Val1217Phe
NM_001318829.1:c.3613G>T NP_001305758.1:p.Val1205Phe
NM_001318829.2:c.3613G>T NP_001305758.1:p.Val1205Phe
NM_001318831.1:c.3226G>T NP_001305760.1:p.Val1076Phe
NM_001318831.2:c.3226G>T NP_001305760.1:p.Val1076Phe
NM_001318832.1:c.3790G>T NP_001305761.1:p.Val1264Phe
NM_001318832.2:c.3790G>T NP_001305761.1:p.Val1264Phe
NM_001363528.1:c.3760G>T NP_001350457.1:p.Val1254Phe
NM_001363528.2:c.3760G>T NP_001350457.1:p.Val1254Phe
NM_001370404.1:c.3826G>T NP_001357333.1:p.Val1276Phe
NM_001370405.1:c.3829G>T NP_001357334.1:p.Val1277Phe
NM_021055.2:c.3829G>T NP_066399.2:p.Val1277Phe
NM_021055.3:c.3829G>T NP_066399.2:p.Val1277Phe
ENST00000219476.7:c.3958G>T ENSP00000219476.3:p.Val1320Phe
ENST00000350773.8:c.3889G>T ENSP00000344383.4:p.Val1297Phe
ENST00000350773.9:c.3889G>T ENSP00000344383.4:p.Val1297Phe
ENST00000382538.10:c.3613G>T ENSP00000371978.6:p.Val1205Phe
ENST00000401874.6:c.3757G>T ENSP00000384468.2:p.Val1253Phe
ENST00000401874.7:c.3757G>T ENSP00000384468.2:p.Val1253Phe
ENST00000439117.6:c.*3125G>T ENSP00000406980.2:n.*3125G>T
ENST00000439673.6:c.3649G>T ENSP00000399232.2:p.Val1217Phe
ENST00000497886.5:n.1716G>T
ENST00000568454.5:c.3790G>T ENSP00000454487.1:p.Val1264Phe
ENST00000568454.6:c.3790G>T ENSP00000454487.1:p.Val1264Phe
ENST00000568566.6:c.*2307G>T ENSP00000455997.2:n.*2307G>T
ENST00000569110.1:c.140G>T
ENST00000569110.2:c.194G>T
ENST00000569930.1:n.1073G>T
ENST00000569930.2:n.1840G>T
ENST00000642206.2:c.3805G>T ENSP00000495146.2:p.Val1269Phe
ENST00000642365.1:c.2612G>T
ENST00000642365.2:c.3955G>T ENSP00000495459.2:p.Val1319Phe
ENST00000642561.1:c.3829G>T ENSP00000495099.1:p.Val1277Phe
ENST00000642728.1:n.140G>T
ENST00000642797.1:c.3760G>T ENSP00000493846.1:p.Val1254Phe
ENST00000642936.1:c.3826G>T ENSP00000494514.1:p.Val1276Phe
ENST00000643088.1:c.3757G>T ENSP00000494747.1:p.Val1253Phe
ENST00000643426.1:n.1606G>T
ENST00000643533.1:n.399G>T
ENST00000643946.1:c.3889G>T ENSP00000495927.1:p.Val1297Phe
ENST00000644043.1:c.3829G>T ENSP00000496262.1:p.Val1277Phe
ENST00000644329.1:c.3757G>T ENSP00000496611.1:p.Val1253Phe
ENST00000644335.1:c.3760G>T ENSP00000496317.1:p.Val1254Phe
ENST00000644399.1:c.3879G>T
ENST00000644417.2:c.*4338G>T ENSP00000493912.2:n.*4338G>T
ENST00000645024.1:n.2042G>T
ENST00000645186.1:c.201G>T
ENST00000646388.1:c.3958G>T ENSP00000495921.1:p.Val1320Phe
ENST00000646464.2:c.*6707G>T ENSP00000496610.2:n.*6707G>T
ENST00000646634.1:n.2773G>T
ENST00000646674.1:n.1210G>T
ENST00000647042.1:n.1181G>T
ENST00000647180.1:n.1071G>T
XM_005255529.3:c.3829G>T XP_005255586.2:p.Val1277Phe
XM_005255531.3:c.3760G>T XP_005255588.2:p.Val1254Phe
XM_005255531.4:c.3760G>T XP_005255588.2:p.Val1254Phe
XM_011522636.1:c.4012G>T XP_011520938.1:p.Val1338Phe
XM_011522636.2:c.4012G>T XP_011520938.1:p.Val1338Phe
XM_011522637.1:c.4009G>T XP_011520939.1:p.Val1337Phe
XM_011522637.2:c.4009G>T XP_011520939.1:p.Val1337Phe
XM_011522638.1:c.3901G>T XP_011520940.1:p.Val1301Phe
XM_011522638.2:c.4174G>T XP_011520940.2:p.Val1392Phe
XM_011522639.1:c.3883G>T XP_011520941.1:p.Val1295Phe
XM_011522639.2:c.3883G>T XP_011520941.1:p.Val1295Phe
XM_011522640.1:c.3880G>T XP_011520942.1:p.Val1294Phe
XM_011522640.2:c.3880G>T XP_011520942.1:p.Val1294Phe
XM_011522641.1:c.3649G>T XP_011520943.1:p.Val1217Phe
XM_017023615.1:c.3955G>T XP_016879104.1:p.Val1319Phe
XM_017023616.1:c.3826G>T XP_016879105.1:p.Val1276Phe
XM_017023617.1:c.3922G>T XP_016879106.1:p.Val1308Phe
XM_017023618.1:c.2668G>T XP_016879107.1:p.Val890Phe
XM_024450413.1:c.3757G>T XP_024306181.1:p.Val1253Phe