Canonical Allele Identifier: CA2202028851
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2079332G= , CM000678.2:g.2079332G= GRCh38
NC_000016.9:g.2129333G= , CM000678.1:g.2129333G= GRCh37
NC_000016.8:g.2069334G= NCBI36
NG_005895.1:g.35027G= , LRG_487:g.35027G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*1606G= ENSP00000455997.2:n.*1606G=
ENST00000642206.2:c.3104G= ENSP00000495146.2:p.Gly1035=
ENST00000642365.2:c.3185G= ENSP00000495459.2:p.Gly1062=
ENST00000644417.2:c.*3637G= ENSP00000493912.2:n.*3637G=
ENST00000646464.2:c.*4110G= ENSP00000496610.2:n.*4110G=
ENST00000219476.9:c.3188G= MANE Select ENSP00000219476.3:p.Gly1063=
ENST00000350773.9:c.3188G= ENSP00000344383.4:p.Gly1063=
ENST00000401874.7:c.3056G= ENSP00000384468.2:p.Gly1019=
ENST00000471143.6:c.416G= ENSP00000458541.2:n.416G=
ENST00000568366.6:n.545G=
ENST00000568454.6:c.3089G= ENSP00000454487.1:p.Gly1030=
ENST00000642365.1:c.1842G=
ENST00000642561.1:c.3059G= ENSP00000495099.1:p.Gly1020=
ENST00000642797.1:c.3059G= ENSP00000493846.1:p.Gly1020=
ENST00000642936.1:c.3056G= ENSP00000494514.1:p.Gly1019=
ENST00000643088.1:c.3056G= ENSP00000494747.1:p.Gly1019=
ENST00000643946.1:c.3188G= ENSP00000495927.1:p.Gly1063=
ENST00000644043.1:c.3059G= ENSP00000496262.1:p.Gly1020=
ENST00000644329.1:c.3056G= ENSP00000496611.1:p.Gly1019=
ENST00000644335.1:c.3059G= ENSP00000496317.1:p.Gly1020=
ENST00000644399.1:c.3178G=
ENST00000644722.1:n.334G=
ENST00000645024.1:n.1341G=
ENST00000646388.1:c.3188G= ENSP00000495921.1:p.Gly1063=
ENST00000646634.1:n.2072G=
ENST00000647042.1:n.480G=
ENST00000219476.7:c.3188G= ENSP00000219476.3:p.Gly1063=
ENST00000350773.8:c.3188G= ENSP00000344383.4:p.Gly1063=
ENST00000382538.10:c.2912G= ENSP00000371978.6:p.Gly971=
ENST00000401874.6:c.3056G= ENSP00000384468.2:p.Gly1019=
ENST00000439117.6:c.*2355G= ENSP00000406980.2:n.*2355G=
ENST00000439673.6:c.2948G= ENSP00000399232.2:p.Gly983=
ENST00000471143.5:c.414G=
ENST00000483020.5:c.428G= ENSP00000460310.1:n.428G=
ENST00000497886.5:n.1015G=
ENST00000561695.1:n.413G=
ENST00000568366.5:n.545G=
ENST00000568454.5:c.3089G= ENSP00000454487.1:p.Gly1030=
NM_000548.3:c.3188G= , LRG_487t1:c.3188G= NP_000539.2:p.Gly1063=
NM_001077183.1:c.3056G= NP_001070651.1:p.Gly1019=
NM_001114382.1:c.3188G= NP_001107854.1:p.Gly1063=
XM_005255529.3:c.3059G= XP_005255586.2:p.Gly1020=
XM_005255531.3:c.3059G= XP_005255588.2:p.Gly1020=
XM_011522636.1:c.3188G= XP_011520938.1:p.Gly1063=
XM_011522637.1:c.3185G= XP_011520939.1:p.Gly1062=
XM_011522638.1:c.3077G= XP_011520940.1:p.Gly1026=
XM_011522639.1:c.3059G= XP_011520941.1:p.Gly1020=
XM_011522640.1:c.3056G= XP_011520942.1:p.Gly1019=
XM_011522641.1:c.2948G= XP_011520943.1:p.Gly983=
NM_000548.4:c.3188G= NP_000539.2:p.Gly1063=
NM_001077183.2:c.3056G= NP_001070651.1:p.Gly1019=
NM_001114382.2:c.3188G= NP_001107854.1:p.Gly1063=
NM_001318827.1:c.2948G= NP_001305756.1:p.Gly983=
NM_001318829.1:c.2912G= NP_001305758.1:p.Gly971=
NM_001318831.1:c.2456G= NP_001305760.1:p.Gly819=
NM_001318832.1:c.3089G= NP_001305761.1:p.Gly1030=
NM_001363528.1:c.3059G= NP_001350457.1:p.Gly1020=
NM_021055.2:c.3059G= NP_066399.2:p.Gly1020=
XM_005255531.4:c.3059G= XP_005255588.2:p.Gly1020=
XM_011522636.2:c.3188G= XP_011520938.1:p.Gly1063=
XM_011522637.2:c.3185G= XP_011520939.1:p.Gly1062=
XM_011522638.2:c.3350G= XP_011520940.2:p.Gly1117=
XM_011522639.2:c.3059G= XP_011520941.1:p.Gly1020=
XM_011522640.2:c.3056G= XP_011520942.1:p.Gly1019=
XM_017023615.1:c.3185G= XP_016879104.1:p.Gly1062=
XM_017023616.1:c.3056G= XP_016879105.1:p.Gly1019=
XM_017023617.1:c.3221G= XP_016879106.1:p.Gly1074=
XM_017023618.1:c.1844G= XP_016879107.1:p.Gly615=
XM_024450413.1:c.3056G= XP_024306181.1:p.Gly1019=
NM_000548.5:c.3188G= MANE Select NP_000539.2:p.Gly1063=
NM_001370404.1:c.3056G= NP_001357333.1:p.Gly1019=
NM_001370405.1:c.3059G= NP_001357334.1:p.Gly1020=
NM_001077183.3:c.3056G= NP_001070651.1:p.Gly1019=
NM_001114382.3:c.3188G= NP_001107854.1:p.Gly1063=
NM_001318827.2:c.2948G= NP_001305756.1:p.Gly983=
NM_001318829.2:c.2912G= NP_001305758.1:p.Gly971=
NM_001318831.2:c.2456G= NP_001305760.1:p.Gly819=
NM_001318832.2:c.3089G= NP_001305761.1:p.Gly1030=
NM_001363528.2:c.3059G= NP_001350457.1:p.Gly1020=
NM_021055.3:c.3059G= NP_066399.2:p.Gly1020=