Canonical Allele Identifier: CA019441
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64878
ClinVar RCV Id: RCV000055078
dbSNP Id: rs397514904

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2081637_2081654del , CM000678.2:g.2081637_2081654del GRCh38
NC_000016.9:g.2131638_2131655del , CM000678.1:g.2131638_2131655del GRCh37
NC_000016.8:g.2071639_2071656del NCBI36
NG_005895.1:g.37332_37349del , LRG_487:g.37332_37349del

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*2071_*2088del ENSP00000455997.2:n.*2071_*2088del
ENST00000642206.2:c.3569_3586del ENSP00000495146.2:p.Pro1190_Asn1196delinsHis
ENST00000642365.2:c.3650_3667del ENSP00000495459.2:p.Pro1217_Asn1223delinsHis
ENST00000644417.2:c.*4102_*4119del ENSP00000493912.2:n.*4102_*4119del
ENST00000646464.2:c.*4575_*4592del ENSP00000496610.2:n.*4575_*4592del
ENST00000219476.9:c.3653_3670del MANE Select ENSP00000219476.3:p.Pro1218_Asn1224delinsHis
ENST00000350773.9:c.3653_3670del ENSP00000344383.4:p.Pro1218_Asn1224delinsHis
ENST00000401874.7:c.3521_3538del ENSP00000384468.2:p.Pro1174_Asn1180delinsHis
ENST00000568454.6:c.3554_3571del ENSP00000454487.1:p.Pro1185_Asn1191delinsHis
ENST00000642365.1:c.2307_2324del
ENST00000642561.1:c.3524_3541del ENSP00000495099.1:p.Pro1175_Asn1181delinsHis
ENST00000642797.1:c.3524_3541del ENSP00000493846.1:p.Pro1175_Asn1181delinsHis
ENST00000642936.1:c.3521_3538del ENSP00000494514.1:p.Pro1174_Asn1180delinsHis
ENST00000643088.1:c.3521_3538del ENSP00000494747.1:p.Pro1174_Asn1180delinsHis
ENST00000643426.1:n.1301_1318del
ENST00000643533.1:n.163_180del
ENST00000643946.1:c.3653_3670del ENSP00000495927.1:p.Pro1218_Asn1224delinsHis
ENST00000644043.1:c.3524_3541del ENSP00000496262.1:p.Pro1175_Asn1181delinsHis
ENST00000644329.1:c.3521_3538del ENSP00000496611.1:p.Pro1174_Asn1180delinsHis
ENST00000644335.1:c.3524_3541del ENSP00000496317.1:p.Pro1175_Asn1181delinsHis
ENST00000644399.1:c.3643_3660del
ENST00000644722.1:n.799_816del
ENST00000645024.1:n.1806_1823del
ENST00000646388.1:c.3653_3670del ENSP00000495921.1:p.Pro1218_Asn1224delinsHis
ENST00000646634.1:n.2537_2554del
ENST00000646674.1:n.268_285del
ENST00000647042.1:n.945_962del
ENST00000647180.1:n.133_150del
ENST00000219476.7:c.3653_3670del ENSP00000219476.3:p.Pro1218_Asn1224delinsHis
ENST00000350773.8:c.3653_3670del ENSP00000344383.4:p.Pro1218_Asn1224delinsHis
ENST00000382538.10:c.3377_3394del ENSP00000371978.6:p.Pro1126_Asn1132delinsHis
ENST00000401874.6:c.3521_3538del ENSP00000384468.2:p.Pro1174_Asn1180delinsHis
ENST00000439117.6:c.*2820_*2837del ENSP00000406980.2:n.*2820_*2837del
ENST00000439673.6:c.3413_3430del ENSP00000399232.2:p.Pro1138_Asn1144delinsHis
ENST00000497886.5:n.1480_1497del
ENST00000568454.5:c.3554_3571del ENSP00000454487.1:p.Pro1185_Asn1191delinsHis
NM_000548.3:c.3653_3670del , LRG_487t1:c.3653_3670del NP_000539.2:p.Pro1218_Asn1224delinsHis
NM_001077183.1:c.3521_3538del NP_001070651.1:p.Pro1174_Asn1180delinsHis
NM_001114382.1:c.3653_3670del NP_001107854.1:p.Pro1218_Asn1224delinsHis
XM_005255529.3:c.3524_3541del XP_005255586.2:p.Pro1175_Asn1181delinsHis
XM_005255531.3:c.3524_3541del XP_005255588.2:p.Pro1175_Asn1181delinsHis
XM_011522636.1:c.3653_3670del XP_011520938.1:p.Pro1218_Asn1224delinsHis
XM_011522637.1:c.3650_3667del XP_011520939.1:p.Pro1217_Asn1223delinsHis
XM_011522638.1:c.3542_3559del XP_011520940.1:p.Pro1181_Asn1187delinsHis
XM_011522639.1:c.3524_3541del XP_011520941.1:p.Pro1175_Asn1181delinsHis
XM_011522640.1:c.3521_3538del XP_011520942.1:p.Pro1174_Asn1180delinsHis
XM_011522641.1:c.3413_3430del XP_011520943.1:p.Pro1138_Asn1144delinsHis
NM_000548.4:c.3653_3670del NP_000539.2:p.Pro1218_Asn1224delinsHis
NM_001077183.2:c.3521_3538del NP_001070651.1:p.Pro1174_Asn1180delinsHis
NM_001114382.2:c.3653_3670del NP_001107854.1:p.Pro1218_Asn1224delinsHis
NM_001318827.1:c.3413_3430del NP_001305756.1:p.Pro1138_Asn1144delinsHis
NM_001318829.1:c.3377_3394del NP_001305758.1:p.Pro1126_Asn1132delinsHis
NM_001318831.1:c.2921_2938del NP_001305760.1:p.Pro974_Asn980delinsHis
NM_001318832.1:c.3554_3571del NP_001305761.1:p.Pro1185_Asn1191delinsHis
NM_001363528.1:c.3524_3541del NP_001350457.1:p.Pro1175_Asn1181delinsHis
NM_021055.2:c.3524_3541del NP_066399.2:p.Pro1175_Asn1181delinsHis
XM_005255531.4:c.3524_3541del XP_005255588.2:p.Pro1175_Asn1181delinsHis
XM_011522636.2:c.3653_3670del XP_011520938.1:p.Pro1218_Asn1224delinsHis
XM_011522637.2:c.3650_3667del XP_011520939.1:p.Pro1217_Asn1223delinsHis
XM_011522638.2:c.3815_3832del XP_011520940.2:p.Pro1272_Asn1278delinsHis
XM_011522639.2:c.3524_3541del XP_011520941.1:p.Pro1175_Asn1181delinsHis
XM_011522640.2:c.3521_3538del XP_011520942.1:p.Pro1174_Asn1180delinsHis
XM_017023615.1:c.3650_3667del XP_016879104.1:p.Pro1217_Asn1223delinsHis
XM_017023616.1:c.3521_3538del XP_016879105.1:p.Pro1174_Asn1180delinsHis
XM_017023617.1:c.3686_3703del XP_016879106.1:p.Pro1229_Asn1235delinsHis
XM_017023618.1:c.2309_2326del XP_016879107.1:p.Pro770_Asn776delinsHis
XM_024450413.1:c.3521_3538del XP_024306181.1:p.Pro1174_Asn1180delinsHis
NM_000548.5:c.3653_3670del MANE Select NP_000539.2:p.Pro1218_Asn1224delinsHis
NM_001370404.1:c.3521_3538del NP_001357333.1:p.Pro1174_Asn1180delinsHis
NM_001370405.1:c.3524_3541del NP_001357334.1:p.Pro1175_Asn1181delinsHis
NM_001077183.3:c.3521_3538del NP_001070651.1:p.Pro1174_Asn1180delinsHis
NM_001114382.3:c.3653_3670del NP_001107854.1:p.Pro1218_Asn1224delinsHis
NM_001318827.2:c.3413_3430del NP_001305756.1:p.Pro1138_Asn1144delinsHis
NM_001318829.2:c.3377_3394del NP_001305758.1:p.Pro1126_Asn1132delinsHis
NM_001318831.2:c.2921_2938del NP_001305760.1:p.Pro974_Asn980delinsHis
NM_001318832.2:c.3554_3571del NP_001305761.1:p.Pro1185_Asn1191delinsHis
NM_001363528.2:c.3524_3541del NP_001350457.1:p.Pro1175_Asn1181delinsHis
NM_021055.3:c.3524_3541del NP_066399.2:p.Pro1175_Asn1181delinsHis