Canonical Allele Identifier: CA2202023060
Gene: TSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2071815_2071855delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC , CM000678.2:g.2071815_2071855delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC GRCh38
NC_000016.9:g.2121816_2121856delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC , CM000678.1:g.2121816_2121856delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC GRCh37
NC_000016.8:g.2061817_2061857delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC NCBI36
NG_005895.1:g.27510_27550delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC , LRG_487:g.27510_27550delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC

Transcript Alleles

HGVS Amino-acid change
ENST00000568566.6:c.*525_*565delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC ENSP00000455997.2:n.*525_*565delinsAGCGGC...
ENST00000642206.2:c.2023_2063delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC ENSP00000495146.2:p.Ser675=
ENST00000642365.2:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC ENSP00000495459.2:p.Ser660=
ENST00000644417.2:c.*1415_*1455delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC ENSP00000493912.2:n.*1415_*1455delinsAGCG...
ENST00000646464.2:c.*1583_*1623delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC ENSP00000496610.2:n.*1583_*1623delinsAGCG...
ENST00000219476.9:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC MANE Select ENSP00000219476.3:p.Ser660=
ENST00000350773.9:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC ENSP00000344383.4:p.Ser660=
ENST00000401874.7:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC ENSP00000384468.2:p.Ser660=
ENST00000563346.2:n.156_196delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC
ENST00000568454.6:c.2011_2051delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC ENSP00000454487.1:p.Ser671=
ENST00000642365.1:c.635_675delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC
ENST00000642561.1:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC ENSP00000495099.1:p.Ser660=
ENST00000642797.1:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC ENSP00000493846.1:p.Ser660=
ENST00000642936.1:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC ENSP00000494514.1:p.Ser660=
ENST00000643088.1:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC ENSP00000494747.1:p.Ser660=
ENST00000643298.1:c.*1480_*1520delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC ENSP00000494393.1:n.*1480_*1520delinsAGCG...
ENST00000643946.1:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC ENSP00000495927.1:p.Ser660=
ENST00000644043.1:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC ENSP00000496262.1:p.Ser660=
ENST00000644329.1:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC ENSP00000496611.1:p.Ser660=
ENST00000644335.1:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC ENSP00000496317.1:p.Ser660=
ENST00000644399.1:c.1971_2011delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC
ENST00000644847.1:n.970_1010delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC
ENST00000645024.1:n.260_300delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC
ENST00000645552.1:n.258_298delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC
ENST00000646388.1:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC ENSP00000495921.1:p.Ser660=
ENST00000646464.1:c.31_71delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC ENSP00000496610.1:p.Ser11=
ENST00000646634.1:n.991_1031delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC
ENST00000219476.7:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC ENSP00000219476.3:p.Ser660=
ENST00000350773.8:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC ENSP00000344383.4:p.Ser660=
ENST00000382538.10:c.1831_1871delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC ENSP00000371978.6:p.Ser611=
ENST00000401874.6:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC ENSP00000384468.2:p.Ser660=
ENST00000439117.6:c.*1277_*1317delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC ENSP00000406980.2:n.*1277_*1317delinsAGCG...
ENST00000439673.6:c.1867_1907delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC ENSP00000399232.2:p.Ser623=
ENST00000488675.5:n.485_525delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC
ENST00000563346.1:n.47_87delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC
ENST00000568454.5:c.2011_2051delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC ENSP00000454487.1:p.Ser671=
NM_000548.3:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC , LRG_487t1:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC NP_000539.2:p.Ser660=
NM_001077183.1:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC NP_001070651.1:p.Ser660=
NM_001114382.1:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC NP_001107854.1:p.Ser660=
XM_005255529.3:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC XP_005255586.2:p.Ser660=
XM_005255531.3:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC XP_005255588.2:p.Ser660=
XM_011522636.1:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC XP_011520938.1:p.Ser660=
XM_011522637.1:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC XP_011520939.1:p.Ser660=
XM_011522638.1:c.1867_1907delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC XP_011520940.1:p.Ser623=
XM_011522639.1:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC XP_011520941.1:p.Ser660=
XM_011522640.1:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC XP_011520942.1:p.Ser660=
XM_011522641.1:c.1867_1907delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC XP_011520943.1:p.Ser623=
NM_000548.4:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC NP_000539.2:p.Ser660=
NM_001077183.2:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC NP_001070651.1:p.Ser660=
NM_001114382.2:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC NP_001107854.1:p.Ser660=
NM_001318827.1:c.1867_1907delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC NP_001305756.1:p.Ser623=
NM_001318829.1:c.1831_1871delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC NP_001305758.1:p.Ser611=
NM_001318831.1:c.1378_1418delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC NP_001305760.1:p.Ser460=
NM_001318832.1:c.2011_2051delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC NP_001305761.1:p.Ser671=
NM_001363528.1:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC NP_001350457.1:p.Ser660=
NM_021055.2:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC NP_066399.2:p.Ser660=
XM_005255531.4:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC XP_005255588.2:p.Ser660=
XM_011522636.2:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC XP_011520938.1:p.Ser660=
XM_011522637.2:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC XP_011520939.1:p.Ser660=
XM_011522638.2:c.2140_2180delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC XP_011520940.2:p.Ser714=
XM_011522639.2:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC XP_011520941.1:p.Ser660=
XM_011522640.2:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC XP_011520942.1:p.Ser660=
XM_017023615.1:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC XP_016879104.1:p.Ser660=
XM_017023616.1:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC XP_016879105.1:p.Ser660=
XM_017023617.1:c.2140_2180delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC XP_016879106.1:p.Ser714=
XM_017023618.1:c.634_674delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC XP_016879107.1:p.Ser212=
XM_024450413.1:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC XP_024306181.1:p.Ser660=
NM_000548.5:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC MANE Select NP_000539.2:p.Ser660=
NM_001370404.1:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC NP_001357333.1:p.Ser660=
NM_001370405.1:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC NP_001357334.1:p.Ser660=
NM_001077183.3:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC NP_001070651.1:p.Ser660=
NM_001114382.3:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC NP_001107854.1:p.Ser660=
NM_001318827.2:c.1867_1907delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC NP_001305756.1:p.Ser623=
NM_001318829.2:c.1831_1871delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC NP_001305758.1:p.Ser611=
NM_001318831.2:c.1378_1418delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC NP_001305760.1:p.Ser460=
NM_001318832.2:c.2011_2051delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC NP_001305761.1:p.Ser671=
NM_001363528.2:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC NP_001350457.1:p.Ser660=
NM_021055.3:c.1978_2018delinsAGCGGCCCCCTTTCTCCTCCCACAGGGCCTCCTGGCCCGGC NP_066399.2:p.Ser660=