Canonical Allele Identifier: CA394299165

Gene: TSC2

Linked Data

• MyVariant Identifiers: chr16:g.2134239T>C (hg19) ; chr16:g.2084238T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2084238T>C , CM000678.2:g.2084238T>C	GRCh38
NC_000016.9:g.2134239T>C , CM000678.1:g.2134239T>C	GRCh37
NC_000016.8:g.2074240T>C	NCBI36
NG_005895.1:g.39933T>C , LRG_487:g.39933T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*2365T>C	ENSP00000455997.2:n.*2365T>C
ENST00000642206.2:c.3863T>C	ENSP00000495146.2:p.Val1288Ala
ENST00000642365.2:c.4013T>C	ENSP00000495459.2:p.Val1338Ala
ENST00000644417.2:c.*4396T>C	ENSP00000493912.2:n.*4396T>C
ENST00000646464.2:c.*6765T>C	ENSP00000496610.2:n.*6765T>C
ENST00000219476.9:c.4016T>C MANE Select	ENSP00000219476.3:p.Val1339Ala
ENST00000350773.9:c.3947T>C	ENSP00000344383.4:p.Val1316Ala
ENST00000401874.7:c.3815T>C	ENSP00000384468.2:p.Val1272Ala
ENST00000568454.6:c.3848T>C	ENSP00000454487.1:p.Val1283Ala
ENST00000569110.2:c.252T>C
ENST00000569930.2:n.1898T>C
ENST00000642365.1:c.2670T>C
ENST00000642561.1:c.3887T>C	ENSP00000495099.1:p.Val1296Ala
ENST00000642728.1:n.198T>C
ENST00000642797.1:c.3818T>C	ENSP00000493846.1:p.Val1273Ala
ENST00000642936.1:c.3884T>C	ENSP00000494514.1:p.Val1295Ala
ENST00000643088.1:c.3815T>C	ENSP00000494747.1:p.Val1272Ala
ENST00000643177.1:n.30T>C
ENST00000643426.1:n.1664T>C
ENST00000643533.1:n.457T>C
ENST00000643946.1:c.3947T>C	ENSP00000495927.1:p.Val1316Ala
ENST00000644043.1:c.3887T>C	ENSP00000496262.1:p.Val1296Ala
ENST00000644329.1:c.3815T>C	ENSP00000496611.1:p.Val1272Ala
ENST00000644335.1:c.3818T>C	ENSP00000496317.1:p.Val1273Ala
ENST00000644399.1:c.3937T>C
ENST00000645024.1:n.2100T>C
ENST00000645186.1:c.259T>C
ENST00000646388.1:c.4016T>C	ENSP00000495921.1:p.Val1339Ala
ENST00000646634.1:n.2831T>C
ENST00000646674.1:n.1268T>C
ENST00000647042.1:n.1239T>C
ENST00000647180.1:n.1129T>C
ENST00000219476.7:c.4016T>C	ENSP00000219476.3:p.Val1339Ala
ENST00000350773.8:c.3947T>C	ENSP00000344383.4:p.Val1316Ala
ENST00000382538.10:c.3671T>C	ENSP00000371978.6:p.Val1224Ala
ENST00000401874.6:c.3815T>C	ENSP00000384468.2:p.Val1272Ala
ENST00000439117.6:c.*3183T>C	ENSP00000406980.2:n.*3183T>C
ENST00000439673.6:c.3707T>C	ENSP00000399232.2:p.Val1236Ala
ENST00000497886.5:n.1774T>C
ENST00000568454.5:c.3848T>C	ENSP00000454487.1:p.Val1283Ala
ENST00000569110.1:c.198T>C
ENST00000569930.1:n.1131T>C
NM_000548.3:c.4016T>C , LRG_487t1:c.4016T>C	NP_000539.2:p.Val1339Ala
NM_001077183.1:c.3815T>C	NP_001070651.1:p.Val1272Ala
NM_001114382.1:c.3947T>C	NP_001107854.1:p.Val1316Ala
XM_005255529.3:c.3887T>C	XP_005255586.2:p.Val1296Ala
XM_005255531.3:c.3818T>C	XP_005255588.2:p.Val1273Ala
XM_011522636.1:c.4070T>C	XP_011520938.1:p.Val1357Ala
XM_011522637.1:c.4067T>C	XP_011520939.1:p.Val1356Ala
XM_011522638.1:c.3959T>C	XP_011520940.1:p.Val1320Ala
XM_011522639.1:c.3941T>C	XP_011520941.1:p.Val1314Ala
XM_011522640.1:c.3938T>C	XP_011520942.1:p.Val1313Ala
XM_011522641.1:c.3707T>C	XP_011520943.1:p.Val1236Ala
NM_000548.4:c.4016T>C	NP_000539.2:p.Val1339Ala
NM_001077183.2:c.3815T>C	NP_001070651.1:p.Val1272Ala
NM_001114382.2:c.3947T>C	NP_001107854.1:p.Val1316Ala
NM_001318827.1:c.3707T>C	NP_001305756.1:p.Val1236Ala
NM_001318829.1:c.3671T>C	NP_001305758.1:p.Val1224Ala
NM_001318831.1:c.3284T>C	NP_001305760.1:p.Val1095Ala
NM_001318832.1:c.3848T>C	NP_001305761.1:p.Val1283Ala
NM_001363528.1:c.3818T>C	NP_001350457.1:p.Val1273Ala
NM_021055.2:c.3887T>C	NP_066399.2:p.Val1296Ala
XM_005255531.4:c.3818T>C	XP_005255588.2:p.Val1273Ala
XM_011522636.2:c.4070T>C	XP_011520938.1:p.Val1357Ala
XM_011522637.2:c.4067T>C	XP_011520939.1:p.Val1356Ala
XM_011522638.2:c.4232T>C	XP_011520940.2:p.Val1411Ala
XM_011522639.2:c.3941T>C	XP_011520941.1:p.Val1314Ala
XM_011522640.2:c.3938T>C	XP_011520942.1:p.Val1313Ala
XM_017023615.1:c.4013T>C	XP_016879104.1:p.Val1338Ala
XM_017023616.1:c.3884T>C	XP_016879105.1:p.Val1295Ala
XM_017023617.1:c.3980T>C	XP_016879106.1:p.Val1327Ala
XM_017023618.1:c.2726T>C	XP_016879107.1:p.Val909Ala
XM_024450413.1:c.3815T>C	XP_024306181.1:p.Val1272Ala
NM_000548.5:c.4016T>C MANE Select	NP_000539.2:p.Val1339Ala
NM_001370404.1:c.3884T>C	NP_001357333.1:p.Val1295Ala
NM_001370405.1:c.3887T>C	NP_001357334.1:p.Val1296Ala
NM_001077183.3:c.3815T>C	NP_001070651.1:p.Val1272Ala
NM_001114382.3:c.3947T>C	NP_001107854.1:p.Val1316Ala
NM_001318827.2:c.3707T>C	NP_001305756.1:p.Val1236Ala
NM_001318829.2:c.3671T>C	NP_001305758.1:p.Val1224Ala
NM_001318831.2:c.3284T>C	NP_001305760.1:p.Val1095Ala
NM_001318832.2:c.3848T>C	NP_001305761.1:p.Val1283Ala
NM_001363528.2:c.3818T>C	NP_001350457.1:p.Val1273Ala
NM_021055.3:c.3887T>C	NP_066399.2:p.Val1296Ala