Canonical Allele Identifier: CA10583318
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238013
ClinVar RCV Id: RCV000228906
dbSNP Id: rs878854091
gnomAD v4: 16-2079299-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2079299T>C , CM000678.2:g.2079299T>C GRCh38
NC_000016.9:g.2129300T>C , CM000678.1:g.2129300T>C GRCh37
NC_000016.8:g.2069301T>C NCBI36
NG_005895.1:g.34994T>C , LRG_487:g.34994T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000568566.6:c.*1573T>C ENSP00000455997.2:n.*1573T>C
ENST00000642206.2:c.3071T>C ENSP00000495146.2:p.Leu1024Pro
ENST00000642365.2:c.3152T>C ENSP00000495459.2:p.Leu1051Pro
ENST00000644417.2:c.*3604T>C ENSP00000493912.2:n.*3604T>C
ENST00000646464.2:c.*4077T>C ENSP00000496610.2:n.*4077T>C
ENST00000219476.9:c.3155T>C MANE Select ENSP00000219476.3:p.Leu1052Pro
ENST00000350773.9:c.3155T>C ENSP00000344383.4:p.Leu1052Pro
ENST00000401874.7:c.3023T>C ENSP00000384468.2:p.Leu1008Pro
ENST00000471143.6:c.383T>C ENSP00000458541.2:n.383T>C
ENST00000568366.6:n.512T>C
ENST00000568454.6:c.3056T>C ENSP00000454487.1:p.Leu1019Pro
ENST00000642365.1:c.1809T>C
ENST00000642561.1:c.3026T>C ENSP00000495099.1:p.Leu1009Pro
ENST00000642797.1:c.3026T>C ENSP00000493846.1:p.Leu1009Pro
ENST00000642936.1:c.3023T>C ENSP00000494514.1:p.Leu1008Pro
ENST00000643088.1:c.3023T>C ENSP00000494747.1:p.Leu1008Pro
ENST00000643946.1:c.3155T>C ENSP00000495927.1:p.Leu1052Pro
ENST00000644043.1:c.3026T>C ENSP00000496262.1:p.Leu1009Pro
ENST00000644329.1:c.3023T>C ENSP00000496611.1:p.Leu1008Pro
ENST00000644335.1:c.3026T>C ENSP00000496317.1:p.Leu1009Pro
ENST00000644399.1:c.3145T>C
ENST00000644722.1:n.301T>C
ENST00000645024.1:n.1308T>C
ENST00000646388.1:c.3155T>C ENSP00000495921.1:p.Leu1052Pro
ENST00000646634.1:n.2039T>C
ENST00000647042.1:n.447T>C
ENST00000219476.7:c.3155T>C ENSP00000219476.3:p.Leu1052Pro
ENST00000350773.8:c.3155T>C ENSP00000344383.4:p.Leu1052Pro
ENST00000382538.10:c.2879T>C ENSP00000371978.6:p.Leu960Pro
ENST00000401874.6:c.3023T>C ENSP00000384468.2:p.Leu1008Pro
ENST00000439117.6:c.*2322T>C ENSP00000406980.2:n.*2322T>C
ENST00000439673.6:c.2915T>C ENSP00000399232.2:p.Leu972Pro
ENST00000471143.5:c.381T>C
ENST00000483020.5:c.395T>C ENSP00000460310.1:n.395T>C
ENST00000497886.5:n.982T>C
ENST00000561695.1:n.380T>C
ENST00000568366.5:n.512T>C
ENST00000568454.5:c.3056T>C ENSP00000454487.1:p.Leu1019Pro
NM_000548.3:c.3155T>C , LRG_487t1:c.3155T>C NP_000539.2:p.Leu1052Pro
NM_001077183.1:c.3023T>C NP_001070651.1:p.Leu1008Pro
NM_001114382.1:c.3155T>C NP_001107854.1:p.Leu1052Pro
XM_005255529.3:c.3026T>C XP_005255586.2:p.Leu1009Pro
XM_005255531.3:c.3026T>C XP_005255588.2:p.Leu1009Pro
XM_011522636.1:c.3155T>C XP_011520938.1:p.Leu1052Pro
XM_011522637.1:c.3152T>C XP_011520939.1:p.Leu1051Pro
XM_011522638.1:c.3044T>C XP_011520940.1:p.Leu1015Pro
XM_011522639.1:c.3026T>C XP_011520941.1:p.Leu1009Pro
XM_011522640.1:c.3023T>C XP_011520942.1:p.Leu1008Pro
XM_011522641.1:c.2915T>C XP_011520943.1:p.Leu972Pro
NM_000548.4:c.3155T>C NP_000539.2:p.Leu1052Pro
NM_001077183.2:c.3023T>C NP_001070651.1:p.Leu1008Pro
NM_001114382.2:c.3155T>C NP_001107854.1:p.Leu1052Pro
NM_001318827.1:c.2915T>C NP_001305756.1:p.Leu972Pro
NM_001318829.1:c.2879T>C NP_001305758.1:p.Leu960Pro
NM_001318831.1:c.2423T>C NP_001305760.1:p.Leu808Pro
NM_001318832.1:c.3056T>C NP_001305761.1:p.Leu1019Pro
NM_001363528.1:c.3026T>C NP_001350457.1:p.Leu1009Pro
NM_021055.2:c.3026T>C NP_066399.2:p.Leu1009Pro
XM_005255531.4:c.3026T>C XP_005255588.2:p.Leu1009Pro
XM_011522636.2:c.3155T>C XP_011520938.1:p.Leu1052Pro
XM_011522637.2:c.3152T>C XP_011520939.1:p.Leu1051Pro
XM_011522638.2:c.3317T>C XP_011520940.2:p.Leu1106Pro
XM_011522639.2:c.3026T>C XP_011520941.1:p.Leu1009Pro
XM_011522640.2:c.3023T>C XP_011520942.1:p.Leu1008Pro
XM_017023615.1:c.3152T>C XP_016879104.1:p.Leu1051Pro
XM_017023616.1:c.3023T>C XP_016879105.1:p.Leu1008Pro
XM_017023617.1:c.3188T>C XP_016879106.1:p.Leu1063Pro
XM_017023618.1:c.1811T>C XP_016879107.1:p.Leu604Pro
XM_024450413.1:c.3023T>C XP_024306181.1:p.Leu1008Pro
NM_000548.5:c.3155T>C MANE Select NP_000539.2:p.Leu1052Pro
NM_001370404.1:c.3023T>C NP_001357333.1:p.Leu1008Pro
NM_001370405.1:c.3026T>C NP_001357334.1:p.Leu1009Pro
NM_001077183.3:c.3023T>C NP_001070651.1:p.Leu1008Pro
NM_001114382.3:c.3155T>C NP_001107854.1:p.Leu1052Pro
NM_001318827.2:c.2915T>C NP_001305756.1:p.Leu972Pro
NM_001318829.2:c.2879T>C NP_001305758.1:p.Leu960Pro
NM_001318831.2:c.2423T>C NP_001305760.1:p.Leu808Pro
NM_001318832.2:c.3056T>C NP_001305761.1:p.Leu1019Pro
NM_001363528.2:c.3026T>C NP_001350457.1:p.Leu1009Pro
NM_021055.3:c.3026T>C NP_066399.2:p.Leu1009Pro