Canonical Allele Identifier: CA017384
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49725
dbSNP Id: rs137853995

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2074254T>C , CM000678.2:g.2074254T>C GRCh38
NC_000016.9:g.2124255T>C , CM000678.1:g.2124255T>C GRCh37
NC_000016.8:g.2064256T>C NCBI36
NG_005895.1:g.29949T>C , LRG_487:g.29949T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*957T>C ENSP00000455997.2:n.*957T>C
ENST00000642206.2:c.2455T>C ENSP00000495146.2:p.Cys819Arg
ENST00000642365.2:c.2410T>C ENSP00000495459.2:p.Cys804Arg
ENST00000644417.2:c.*1847T>C ENSP00000493912.2:n.*1847T>C
ENST00000646464.2:c.*2055T>C ENSP00000496610.2:n.*2055T>C
ENST00000219476.9:c.2410T>C MANE Select ENSP00000219476.3:p.Cys804Arg
ENST00000350773.9:c.2410T>C ENSP00000344383.4:p.Cys804Arg
ENST00000401874.7:c.2410T>C ENSP00000384468.2:p.Cys804Arg
ENST00000563346.2:n.588T>C
ENST00000568454.6:c.2443T>C ENSP00000454487.1:p.Cys815Arg
ENST00000642365.1:c.1067T>C
ENST00000642561.1:c.2410T>C ENSP00000495099.1:p.Cys804Arg
ENST00000642797.1:c.2410T>C ENSP00000493846.1:p.Cys804Arg
ENST00000642936.1:c.2410T>C ENSP00000494514.1:p.Cys804Arg
ENST00000643088.1:c.2410T>C ENSP00000494747.1:p.Cys804Arg
ENST00000643298.1:c.*1912T>C ENSP00000494393.1:n.*1912T>C
ENST00000643946.1:c.2410T>C ENSP00000495927.1:p.Cys804Arg
ENST00000644043.1:c.2410T>C ENSP00000496262.1:p.Cys804Arg
ENST00000644329.1:c.2410T>C ENSP00000496611.1:p.Cys804Arg
ENST00000644335.1:c.2410T>C ENSP00000496317.1:p.Cys804Arg
ENST00000644399.1:c.2403T>C
ENST00000644847.1:n.1402T>C
ENST00000645024.1:n.692T>C
ENST00000645552.1:n.690T>C
ENST00000646388.1:c.2410T>C ENSP00000495921.1:p.Cys804Arg
ENST00000646634.1:n.1423T>C
ENST00000219476.7:c.2410T>C ENSP00000219476.3:p.Cys804Arg
ENST00000350773.8:c.2410T>C ENSP00000344383.4:p.Cys804Arg
ENST00000382538.10:c.2263T>C ENSP00000371978.6:p.Cys755Arg
ENST00000401874.6:c.2410T>C ENSP00000384468.2:p.Cys804Arg
ENST00000439117.6:c.*1709T>C ENSP00000406980.2:n.*1709T>C
ENST00000439673.6:c.2299T>C ENSP00000399232.2:p.Cys767Arg
ENST00000463808.1:n.444T>C
ENST00000563346.1:n.479T>C
ENST00000568454.5:c.2443T>C ENSP00000454487.1:p.Cys815Arg
NM_000548.3:c.2410T>C , LRG_487t1:c.2410T>C NP_000539.2:p.Cys804Arg
NM_001077183.1:c.2410T>C NP_001070651.1:p.Cys804Arg
NM_001114382.1:c.2410T>C NP_001107854.1:p.Cys804Arg
XM_005255529.3:c.2410T>C XP_005255586.2:p.Cys804Arg
XM_005255531.3:c.2410T>C XP_005255588.2:p.Cys804Arg
XM_011522636.1:c.2410T>C XP_011520938.1:p.Cys804Arg
XM_011522637.1:c.2410T>C XP_011520939.1:p.Cys804Arg
XM_011522638.1:c.2299T>C XP_011520940.1:p.Cys767Arg
XM_011522639.1:c.2410T>C XP_011520941.1:p.Cys804Arg
XM_011522640.1:c.2410T>C XP_011520942.1:p.Cys804Arg
XM_011522641.1:c.2299T>C XP_011520943.1:p.Cys767Arg
NM_000548.4:c.2410T>C NP_000539.2:p.Cys804Arg
NM_001077183.2:c.2410T>C NP_001070651.1:p.Cys804Arg
NM_001114382.2:c.2410T>C NP_001107854.1:p.Cys804Arg
NM_001318827.1:c.2299T>C NP_001305756.1:p.Cys767Arg
NM_001318829.1:c.2263T>C NP_001305758.1:p.Cys755Arg
NM_001318831.1:c.1810T>C NP_001305760.1:p.Cys604Arg
NM_001318832.1:c.2443T>C NP_001305761.1:p.Cys815Arg
NM_001363528.1:c.2410T>C NP_001350457.1:p.Cys804Arg
NM_021055.2:c.2410T>C NP_066399.2:p.Cys804Arg
XM_005255531.4:c.2410T>C XP_005255588.2:p.Cys804Arg
XM_011522636.2:c.2410T>C XP_011520938.1:p.Cys804Arg
XM_011522637.2:c.2410T>C XP_011520939.1:p.Cys804Arg
XM_011522638.2:c.2572T>C XP_011520940.2:p.Cys858Arg
XM_011522639.2:c.2410T>C XP_011520941.1:p.Cys804Arg
XM_011522640.2:c.2410T>C XP_011520942.1:p.Cys804Arg
XM_017023615.1:c.2410T>C XP_016879104.1:p.Cys804Arg
XM_017023616.1:c.2410T>C XP_016879105.1:p.Cys804Arg
XM_017023617.1:c.2572T>C XP_016879106.1:p.Cys858Arg
XM_017023618.1:c.1066T>C XP_016879107.1:p.Cys356Arg
XM_024450413.1:c.2410T>C XP_024306181.1:p.Cys804Arg
NM_000548.5:c.2410T>C MANE Select NP_000539.2:p.Cys804Arg
NM_001370404.1:c.2410T>C NP_001357333.1:p.Cys804Arg
NM_001370405.1:c.2410T>C NP_001357334.1:p.Cys804Arg
NM_001077183.3:c.2410T>C NP_001070651.1:p.Cys804Arg
NM_001114382.3:c.2410T>C NP_001107854.1:p.Cys804Arg
NM_001318827.2:c.2299T>C NP_001305756.1:p.Cys767Arg
NM_001318829.2:c.2263T>C NP_001305758.1:p.Cys755Arg
NM_001318831.2:c.1810T>C NP_001305760.1:p.Cys604Arg
NM_001318832.2:c.2443T>C NP_001305761.1:p.Cys815Arg
NM_001363528.2:c.2410T>C NP_001350457.1:p.Cys804Arg
NM_021055.3:c.2410T>C NP_066399.2:p.Cys804Arg