Canonical Allele Identifier: CA2731832988
Gene: TSC2 HGNC NCBI

Linked Data

dbSNP Id: rs2151350659

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2074274_2074275insATT , CM000678.2:g.2074274_2074275insATT GRCh38
NC_000016.9:g.2124275_2124276insATT , CM000678.1:g.2124275_2124276insATT GRCh37
NC_000016.8:g.2064276_2064277insATT NCBI36
NG_005895.1:g.29969_29970insATT , LRG_487:g.29969_29970insATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*977_*978insATT ENSP00000455997.2:n.*977_*978insATT
ENST00000642206.2:c.2475_2476insATT ENSP00000495146.2:p.Ile825_Cys826insIle
ENST00000642365.2:c.2430_2431insATT ENSP00000495459.2:p.Ile810_Cys811insIle
ENST00000644417.2:c.*1867_*1868insATT ENSP00000493912.2:n.*1867_*1868insATT
ENST00000646464.2:c.*2075_*2076insATT ENSP00000496610.2:n.*2075_*2076insATT
ENST00000219476.9:c.2430_2431insATT MANE Select ENSP00000219476.3:p.Ile810_Cys811insIle
ENST00000350773.9:c.2430_2431insATT ENSP00000344383.4:p.Ile810_Cys811insIle
ENST00000401874.7:c.2430_2431insATT ENSP00000384468.2:p.Ile810_Cys811insIle
ENST00000563346.2:n.608_609insATT
ENST00000568454.6:c.2463_2464insATT ENSP00000454487.1:p.Ile821_Cys822insIle
ENST00000642365.1:c.1087_1088insATT
ENST00000642561.1:c.2430_2431insATT ENSP00000495099.1:p.Ile810_Cys811insIle
ENST00000642797.1:c.2430_2431insATT ENSP00000493846.1:p.Ile810_Cys811insIle
ENST00000642936.1:c.2430_2431insATT ENSP00000494514.1:p.Ile810_Cys811insIle
ENST00000643088.1:c.2430_2431insATT ENSP00000494747.1:p.Ile810_Cys811insIle
ENST00000643298.1:c.*1932_*1933insATT ENSP00000494393.1:n.*1932_*1933insATT
ENST00000643946.1:c.2430_2431insATT ENSP00000495927.1:p.Ile810_Cys811insIle
ENST00000644043.1:c.2430_2431insATT ENSP00000496262.1:p.Ile810_Cys811insIle
ENST00000644329.1:c.2430_2431insATT ENSP00000496611.1:p.Ile810_Cys811insIle
ENST00000644335.1:c.2430_2431insATT ENSP00000496317.1:p.Ile810_Cys811insIle
ENST00000644399.1:c.2423_2424insATT
ENST00000644847.1:n.1422_1423insATT
ENST00000645024.1:n.712_713insATT
ENST00000645552.1:n.710_711insATT
ENST00000646388.1:c.2430_2431insATT ENSP00000495921.1:p.Ile810_Cys811insIle
ENST00000646634.1:n.1443_1444insATT
ENST00000219476.7:c.2430_2431insATT ENSP00000219476.3:p.Ile810_Cys811insIle
ENST00000350773.8:c.2430_2431insATT ENSP00000344383.4:p.Ile810_Cys811insIle
ENST00000382538.10:c.2283_2284insATT ENSP00000371978.6:p.Ile761_Cys762insIle
ENST00000401874.6:c.2430_2431insATT ENSP00000384468.2:p.Ile810_Cys811insIle
ENST00000439117.6:c.*1729_*1730insATT ENSP00000406980.2:n.*1729_*1730insATT
ENST00000439673.6:c.2319_2320insATT ENSP00000399232.2:p.Ile773_Cys774insIle
ENST00000463808.1:n.464_465insATT
ENST00000563346.1:n.499_500insATT
ENST00000568454.5:c.2463_2464insATT ENSP00000454487.1:p.Ile821_Cys822insIle
NM_000548.3:c.2430_2431insATT , LRG_487t1:c.2430_2431insATT NP_000539.2:p.Ile810_Cys811insIle
NM_001077183.1:c.2430_2431insATT NP_001070651.1:p.Ile810_Cys811insIle
NM_001114382.1:c.2430_2431insATT NP_001107854.1:p.Ile810_Cys811insIle
XM_005255529.3:c.2430_2431insATT XP_005255586.2:p.Ile810_Cys811insIle
XM_005255531.3:c.2430_2431insATT XP_005255588.2:p.Ile810_Cys811insIle
XM_011522636.1:c.2430_2431insATT XP_011520938.1:p.Ile810_Cys811insIle
XM_011522637.1:c.2430_2431insATT XP_011520939.1:p.Ile810_Cys811insIle
XM_011522638.1:c.2319_2320insATT XP_011520940.1:p.Ile773_Cys774insIle
XM_011522639.1:c.2430_2431insATT XP_011520941.1:p.Ile810_Cys811insIle
XM_011522640.1:c.2430_2431insATT XP_011520942.1:p.Ile810_Cys811insIle
XM_011522641.1:c.2319_2320insATT XP_011520943.1:p.Ile773_Cys774insIle
NM_000548.4:c.2430_2431insATT NP_000539.2:p.Ile810_Cys811insIle
NM_001077183.2:c.2430_2431insATT NP_001070651.1:p.Ile810_Cys811insIle
NM_001114382.2:c.2430_2431insATT NP_001107854.1:p.Ile810_Cys811insIle
NM_001318827.1:c.2319_2320insATT NP_001305756.1:p.Ile773_Cys774insIle
NM_001318829.1:c.2283_2284insATT NP_001305758.1:p.Ile761_Cys762insIle
NM_001318831.1:c.1830_1831insATT NP_001305760.1:p.Ile610_Cys611insIle
NM_001318832.1:c.2463_2464insATT NP_001305761.1:p.Ile821_Cys822insIle
NM_001363528.1:c.2430_2431insATT NP_001350457.1:p.Ile810_Cys811insIle
NM_021055.2:c.2430_2431insATT NP_066399.2:p.Ile810_Cys811insIle
XM_005255531.4:c.2430_2431insATT XP_005255588.2:p.Ile810_Cys811insIle
XM_011522636.2:c.2430_2431insATT XP_011520938.1:p.Ile810_Cys811insIle
XM_011522637.2:c.2430_2431insATT XP_011520939.1:p.Ile810_Cys811insIle
XM_011522638.2:c.2592_2593insATT XP_011520940.2:p.Ile864_Cys865insIle
XM_011522639.2:c.2430_2431insATT XP_011520941.1:p.Ile810_Cys811insIle
XM_011522640.2:c.2430_2431insATT XP_011520942.1:p.Ile810_Cys811insIle
XM_017023615.1:c.2430_2431insATT XP_016879104.1:p.Ile810_Cys811insIle
XM_017023616.1:c.2430_2431insATT XP_016879105.1:p.Ile810_Cys811insIle
XM_017023617.1:c.2592_2593insATT XP_016879106.1:p.Ile864_Cys865insIle
XM_017023618.1:c.1086_1087insATT XP_016879107.1:p.Ile362_Cys363insIle
XM_024450413.1:c.2430_2431insATT XP_024306181.1:p.Ile810_Cys811insIle
NM_000548.5:c.2430_2431insATT MANE Select NP_000539.2:p.Ile810_Cys811insIle
NM_001370404.1:c.2430_2431insATT NP_001357333.1:p.Ile810_Cys811insIle
NM_001370405.1:c.2430_2431insATT NP_001357334.1:p.Ile810_Cys811insIle
NM_001077183.3:c.2430_2431insATT NP_001070651.1:p.Ile810_Cys811insIle
NM_001114382.3:c.2430_2431insATT NP_001107854.1:p.Ile810_Cys811insIle
NM_001318827.2:c.2319_2320insATT NP_001305756.1:p.Ile773_Cys774insIle
NM_001318829.2:c.2283_2284insATT NP_001305758.1:p.Ile761_Cys762insIle
NM_001318831.2:c.1830_1831insATT NP_001305760.1:p.Ile610_Cys611insIle
NM_001318832.2:c.2463_2464insATT NP_001305761.1:p.Ile821_Cys822insIle
NM_001363528.2:c.2430_2431insATT NP_001350457.1:p.Ile810_Cys811insIle
NM_021055.3:c.2430_2431insATT NP_066399.2:p.Ile810_Cys811insIle