Canonical Allele Identifier: CA2202028003
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2079184C= , CM000678.2:g.2079184C= GRCh38
NC_000016.9:g.2129185C= , CM000678.1:g.2129185C= GRCh37
NC_000016.8:g.2069186C= NCBI36
NG_005895.1:g.34879C= , LRG_487:g.34879C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*1537C= ENSP00000455997.2:n.*1537C=
ENST00000642206.2:c.3035C= ENSP00000495146.2:p.Ala1012=
ENST00000642365.2:c.3116C= ENSP00000495459.2:p.Ala1039=
ENST00000644417.2:c.*3568C= ENSP00000493912.2:n.*3568C=
ENST00000646464.2:c.*4041C= ENSP00000496610.2:n.*4041C=
ENST00000219476.9:c.3119C= MANE Select ENSP00000219476.3:p.Ala1040=
ENST00000350773.9:c.3119C= ENSP00000344383.4:p.Ala1040=
ENST00000401874.7:c.2987C= ENSP00000384468.2:p.Ala996=
ENST00000471143.6:c.347C= ENSP00000458541.2:n.347C=
ENST00000568366.6:n.476C=
ENST00000568454.6:c.3020C= ENSP00000454487.1:p.Ala1007=
ENST00000642365.1:c.1773C=
ENST00000642561.1:c.2990C= ENSP00000495099.1:p.Ala997=
ENST00000642797.1:c.2990C= ENSP00000493846.1:p.Ala997=
ENST00000642936.1:c.2987C= ENSP00000494514.1:p.Ala996=
ENST00000643088.1:c.2987C= ENSP00000494747.1:p.Ala996=
ENST00000643946.1:c.3119C= ENSP00000495927.1:p.Ala1040=
ENST00000644043.1:c.2990C= ENSP00000496262.1:p.Ala997=
ENST00000644329.1:c.2987C= ENSP00000496611.1:p.Ala996=
ENST00000644335.1:c.2990C= ENSP00000496317.1:p.Ala997=
ENST00000644399.1:c.3109C=
ENST00000644722.1:n.265C=
ENST00000645024.1:n.1272C=
ENST00000646388.1:c.3119C= ENSP00000495921.1:p.Ala1040=
ENST00000646634.1:n.2003C=
ENST00000647042.1:n.411C=
ENST00000219476.7:c.3119C= ENSP00000219476.3:p.Ala1040=
ENST00000350773.8:c.3119C= ENSP00000344383.4:p.Ala1040=
ENST00000382538.10:c.2843C= ENSP00000371978.6:p.Ala948=
ENST00000401874.6:c.2987C= ENSP00000384468.2:p.Ala996=
ENST00000439117.6:c.*2286C= ENSP00000406980.2:n.*2286C=
ENST00000439673.6:c.2879C= ENSP00000399232.2:p.Ala960=
ENST00000471143.5:c.345C=
ENST00000483020.5:c.359C= ENSP00000460310.1:n.359C=
ENST00000497886.5:n.946C=
ENST00000561695.1:n.265C=
ENST00000568366.5:n.476C=
ENST00000568454.5:c.3020C= ENSP00000454487.1:p.Ala1007=
NM_000548.3:c.3119C= , LRG_487t1:c.3119C= NP_000539.2:p.Ala1040=
NM_001077183.1:c.2987C= NP_001070651.1:p.Ala996=
NM_001114382.1:c.3119C= NP_001107854.1:p.Ala1040=
XM_005255529.3:c.2990C= XP_005255586.2:p.Ala997=
XM_005255531.3:c.2990C= XP_005255588.2:p.Ala997=
XM_011522636.1:c.3119C= XP_011520938.1:p.Ala1040=
XM_011522637.1:c.3116C= XP_011520939.1:p.Ala1039=
XM_011522638.1:c.3008C= XP_011520940.1:p.Ala1003=
XM_011522639.1:c.2990C= XP_011520941.1:p.Ala997=
XM_011522640.1:c.2987C= XP_011520942.1:p.Ala996=
XM_011522641.1:c.2879C= XP_011520943.1:p.Ala960=
NM_000548.4:c.3119C= NP_000539.2:p.Ala1040=
NM_001077183.2:c.2987C= NP_001070651.1:p.Ala996=
NM_001114382.2:c.3119C= NP_001107854.1:p.Ala1040=
NM_001318827.1:c.2879C= NP_001305756.1:p.Ala960=
NM_001318829.1:c.2843C= NP_001305758.1:p.Ala948=
NM_001318831.1:c.2387C= NP_001305760.1:p.Ala796=
NM_001318832.1:c.3020C= NP_001305761.1:p.Ala1007=
NM_001363528.1:c.2990C= NP_001350457.1:p.Ala997=
NM_021055.2:c.2990C= NP_066399.2:p.Ala997=
XM_005255531.4:c.2990C= XP_005255588.2:p.Ala997=
XM_011522636.2:c.3119C= XP_011520938.1:p.Ala1040=
XM_011522637.2:c.3116C= XP_011520939.1:p.Ala1039=
XM_011522638.2:c.3281C= XP_011520940.2:p.Ala1094=
XM_011522639.2:c.2990C= XP_011520941.1:p.Ala997=
XM_011522640.2:c.2987C= XP_011520942.1:p.Ala996=
XM_017023615.1:c.3116C= XP_016879104.1:p.Ala1039=
XM_017023616.1:c.2987C= XP_016879105.1:p.Ala996=
XM_017023617.1:c.3152C= XP_016879106.1:p.Ala1051=
XM_017023618.1:c.1775C= XP_016879107.1:p.Ala592=
XM_024450413.1:c.2987C= XP_024306181.1:p.Ala996=
NM_000548.5:c.3119C= MANE Select NP_000539.2:p.Ala1040=
NM_001370404.1:c.2987C= NP_001357333.1:p.Ala996=
NM_001370405.1:c.2990C= NP_001357334.1:p.Ala997=
NM_001077183.3:c.2987C= NP_001070651.1:p.Ala996=
NM_001114382.3:c.3119C= NP_001107854.1:p.Ala1040=
NM_001318827.2:c.2879C= NP_001305756.1:p.Ala960=
NM_001318829.2:c.2843C= NP_001305758.1:p.Ala948=
NM_001318831.2:c.2387C= NP_001305760.1:p.Ala796=
NM_001318832.2:c.3020C= NP_001305761.1:p.Ala1007=
NM_001363528.2:c.2990C= NP_001350457.1:p.Ala997=
NM_021055.3:c.2990C= NP_066399.2:p.Ala997=