Canonical Allele Identifier: CA394320813

Gene: TSC2

Linked Data

• gnomAD v4: 16-2061955-G-C
• MyVariant Identifiers: chr16:g.2111956G>C (hg19) ; chr16:g.2061955G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2061955G>C , CM000678.2:g.2061955G>C	GRCh38
NC_000016.9:g.2111956G>C , CM000678.1:g.2111956G>C	GRCh37
NC_000016.8:g.2051957G>C	NCBI36
NG_005895.1:g.17650G>C , LRG_487:g.17650G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.1204G>C	ENSP00000455997.2:p.Gly402Arg
ENST00000642206.2:c.1249G>C	ENSP00000495146.2:p.Gly417Arg
ENST00000642365.2:c.1204G>C	ENSP00000495459.2:p.Gly402Arg
ENST00000644417.2:c.*641G>C	ENSP00000493912.2:n.*641G>C
ENST00000646464.2:c.*809G>C	ENSP00000496610.2:n.*809G>C
ENST00000219476.9:c.1204G>C MANE Select	ENSP00000219476.3:p.Gly402Arg
ENST00000350773.9:c.1204G>C	ENSP00000344383.4:p.Gly402Arg
ENST00000401874.7:c.1204G>C	ENSP00000384468.2:p.Gly402Arg
ENST00000463601.2:n.114G>C
ENST00000467949.2:n.428-542G>C
ENST00000568454.6:c.1237G>C	ENSP00000454487.1:p.Gly413Arg
ENST00000642561.1:c.1204G>C	ENSP00000495099.1:p.Gly402Arg
ENST00000642797.1:c.1204G>C	ENSP00000493846.1:p.Gly402Arg
ENST00000642812.1:n.1249G>C
ENST00000642936.1:c.1204G>C	ENSP00000494514.1:p.Gly402Arg
ENST00000643088.1:c.1204G>C	ENSP00000494747.1:p.Gly402Arg
ENST00000643149.1:n.3214G>C
ENST00000643298.1:c.*706G>C	ENSP00000494393.1:n.*706G>C
ENST00000643745.1:c.*136G>C	ENSP00000495948.1:n.*136G>C
ENST00000643946.1:c.1204G>C	ENSP00000495927.1:p.Gly402Arg
ENST00000644043.1:c.1204G>C	ENSP00000496262.1:p.Gly402Arg
ENST00000644135.1:c.1204G>C	ENSP00000495644.1:p.Gly402Arg
ENST00000644222.1:n.1291G>C
ENST00000644329.1:c.1204G>C	ENSP00000496611.1:p.Gly402Arg
ENST00000644335.1:c.1204G>C	ENSP00000496317.1:p.Gly402Arg
ENST00000644399.1:c.1197G>C
ENST00000644665.1:n.2378G>C
ENST00000644847.1:n.196G>C
ENST00000645591.1:n.2262G>C
ENST00000646388.1:c.1204G>C	ENSP00000495921.1:p.Gly402Arg
ENST00000646634.1:n.217G>C
ENST00000647234.1:n.2962G>C
ENST00000647242.1:n.1872G>C
ENST00000219476.7:c.1204G>C	ENSP00000219476.3:p.Gly402Arg
ENST00000350773.8:c.1204G>C	ENSP00000344383.4:p.Gly402Arg
ENST00000382538.10:c.1057G>C	ENSP00000371978.6:p.Gly353Arg
ENST00000401874.6:c.1204G>C	ENSP00000384468.2:p.Gly402Arg
ENST00000439117.6:c.*503G>C	ENSP00000406980.2:n.*503G>C
ENST00000439673.6:c.1093G>C	ENSP00000399232.2:p.Gly365Arg
ENST00000463601.1:n.367G>C
ENST00000467949.1:c.412-542G>C	ENSP00000454997.1:n.412-542G>C
ENST00000568454.5:c.1237G>C	ENSP00000454487.1:p.Gly413Arg
NM_000548.3:c.1204G>C , LRG_487t1:c.1204G>C	NP_000539.2:p.Gly402Arg
NM_001077183.1:c.1204G>C	NP_001070651.1:p.Gly402Arg
NM_001114382.1:c.1204G>C	NP_001107854.1:p.Gly402Arg
XM_005255529.3:c.1204G>C	XP_005255586.2:p.Gly402Arg
XM_005255531.3:c.1204G>C	XP_005255588.2:p.Gly402Arg
XM_011522636.1:c.1204G>C	XP_011520938.1:p.Gly402Arg
XM_011522637.1:c.1204G>C	XP_011520939.1:p.Gly402Arg
XM_011522638.1:c.1093G>C	XP_011520940.1:p.Gly365Arg
XM_011522639.1:c.1204G>C	XP_011520941.1:p.Gly402Arg
XM_011522640.1:c.1204G>C	XP_011520942.1:p.Gly402Arg
XM_011522641.1:c.1093G>C	XP_011520943.1:p.Gly365Arg
NM_000548.4:c.1204G>C	NP_000539.2:p.Gly402Arg
NM_001077183.2:c.1204G>C	NP_001070651.1:p.Gly402Arg
NM_001114382.2:c.1204G>C	NP_001107854.1:p.Gly402Arg
NM_001318827.1:c.1093G>C	NP_001305756.1:p.Gly365Arg
NM_001318829.1:c.1057G>C	NP_001305758.1:p.Gly353Arg
NM_001318831.1:c.604G>C	NP_001305760.1:p.Gly202Arg
NM_001318832.1:c.1237G>C	NP_001305761.1:p.Gly413Arg
NM_001363528.1:c.1204G>C	NP_001350457.1:p.Gly402Arg
NM_021055.2:c.1204G>C	NP_066399.2:p.Gly402Arg
XM_005255531.4:c.1204G>C	XP_005255588.2:p.Gly402Arg
XM_011522636.2:c.1204G>C	XP_011520938.1:p.Gly402Arg
XM_011522637.2:c.1204G>C	XP_011520939.1:p.Gly402Arg
XM_011522638.2:c.1366G>C	XP_011520940.2:p.Gly456Arg
XM_011522639.2:c.1204G>C	XP_011520941.1:p.Gly402Arg
XM_011522640.2:c.1204G>C	XP_011520942.1:p.Gly402Arg
XM_017023615.1:c.1204G>C	XP_016879104.1:p.Gly402Arg
XM_017023616.1:c.1204G>C	XP_016879105.1:p.Gly402Arg
XM_017023617.1:c.1366G>C	XP_016879106.1:p.Gly456Arg
XM_017023618.1:c.-141G>C	XP_016879107.1:n.-141G>C
XM_024450413.1:c.1204G>C	XP_024306181.1:p.Gly402Arg
NM_000548.5:c.1204G>C MANE Select	NP_000539.2:p.Gly402Arg
NM_001370404.1:c.1204G>C	NP_001357333.1:p.Gly402Arg
NM_001370405.1:c.1204G>C	NP_001357334.1:p.Gly402Arg
NM_001077183.3:c.1204G>C	NP_001070651.1:p.Gly402Arg
NM_001114382.3:c.1204G>C	NP_001107854.1:p.Gly402Arg
NM_001318827.2:c.1093G>C	NP_001305756.1:p.Gly365Arg
NM_001318829.2:c.1057G>C	NP_001305758.1:p.Gly353Arg
NM_001318831.2:c.604G>C	NP_001305760.1:p.Gly202Arg
NM_001318832.2:c.1237G>C	NP_001305761.1:p.Gly413Arg
NM_001363528.2:c.1204G>C	NP_001350457.1:p.Gly402Arg
NM_021055.3:c.1204G>C	NP_066399.2:p.Gly402Arg