Canonical Allele Identifier: CA16042990

Gene: TSC2

Linked Data

• ClinVar Variation Id: 373118
• ClinVar RCV Id: RCV000412742 ; RCV001797714
• dbSNP Id: rs1057518230
• MyVariant Identifiers: chr16:g.2134717G>A (hg19) ; chr16:g.2084716G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2084716G>A , CM000678.2:g.2084716G>A	GRCh38
NC_000016.9:g.2134717G>A , CM000678.1:g.2134717G>A	GRCh37
NC_000016.8:g.2074718G>A	NCBI36
NG_005895.1:g.40411G>A , LRG_487:g.40411G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*2842+1G>A	ENSP00000455997.2:n.*2842+1G>A
ENST00000642206.2:c.4340+1G>A	ENSP00000495146.2:n.4340+1G>A
ENST00000642365.2:c.4490+1G>A	ENSP00000495459.2:n.4490+1G>A
ENST00000644417.2:c.*4873+1G>A	ENSP00000493912.2:n.*4873+1G>A
ENST00000646464.2:c.*7242+1G>A	ENSP00000496610.2:n.*7242+1G>A
ENST00000219476.9:c.4493+1G>A MANE Select	ENSP00000219476.3:n.4493+1G>A
ENST00000350773.9:c.4424+1G>A	ENSP00000344383.4:n.4424+1G>A
ENST00000401874.7:c.4292+1G>A	ENSP00000384468.2:n.4292+1G>A
ENST00000568454.6:c.4325+1G>A	ENSP00000454487.1:n.4325+1G>A
ENST00000569110.2:c.716+14G>A
ENST00000569930.2:n.2375+1G>A
ENST00000642365.1:c.3147+1G>A
ENST00000642561.1:c.4364+1G>A	ENSP00000495099.1:n.4364+1G>A
ENST00000642728.1:n.675+1G>A
ENST00000642797.1:c.4295+1G>A	ENSP00000493846.1:n.4295+1G>A
ENST00000642936.1:c.4361+1G>A	ENSP00000494514.1:n.4361+1G>A
ENST00000643088.1:c.4292+1G>A	ENSP00000494747.1:n.4292+1G>A
ENST00000643177.1:n.507+1G>A
ENST00000643426.1:n.2141+1G>A
ENST00000643946.1:c.4424+1G>A	ENSP00000495927.1:n.4424+1G>A
ENST00000644043.1:c.4364+1G>A	ENSP00000496262.1:n.4364+1G>A
ENST00000644329.1:c.4292+1G>A	ENSP00000496611.1:n.4292+1G>A
ENST00000644335.1:c.4295+1G>A	ENSP00000496317.1:n.4295+1G>A
ENST00000644399.1:c.4414+1G>A
ENST00000645024.1:n.2577+1G>A
ENST00000646388.1:c.4493+1G>A	ENSP00000495921.1:n.4493+1G>A
ENST00000646634.1:n.3308+1G>A
ENST00000646674.1:n.1745+1G>A
ENST00000647042.1:n.1716+1G>A
ENST00000647180.1:n.1606+1G>A
ENST00000219476.7:c.4493+1G>A	ENSP00000219476.3:n.4493+1G>A
ENST00000350773.8:c.4424+1G>A	ENSP00000344383.4:n.4424+1G>A
ENST00000382538.10:c.4148+1G>A	ENSP00000371978.6:n.4148+1G>A
ENST00000401874.6:c.4292+1G>A	ENSP00000384468.2:n.4292+1G>A
ENST00000439117.6:c.*3660+1G>A	ENSP00000406980.2:n.*3660+1G>A
ENST00000439673.6:c.4184+1G>A	ENSP00000399232.2:n.4184+1G>A
ENST00000497886.5:n.2251+1G>A
ENST00000568454.5:c.4325+1G>A	ENSP00000454487.1:n.4325+1G>A
ENST00000569110.1:c.675+1G>A
ENST00000569930.1:n.1608+1G>A
NM_000548.3:c.4493+1G>A , LRG_487t1:c.4493+1G>A	NP_000539.2:n.4493+1G>A
NM_001077183.1:c.4292+1G>A	NP_001070651.1:n.4292+1G>A
NM_001114382.1:c.4424+1G>A	NP_001107854.1:n.4424+1G>A
XM_005255529.3:c.4364+1G>A	XP_005255586.2:n.4364+1G>A
XM_005255531.3:c.4295+1G>A	XP_005255588.2:n.4295+1G>A
XM_011522636.1:c.4547+1G>A	XP_011520938.1:n.4547+1G>A
XM_011522637.1:c.4544+1G>A	XP_011520939.1:n.4544+1G>A
XM_011522638.1:c.4436+1G>A	XP_011520940.1:n.4436+1G>A
XM_011522639.1:c.4418+1G>A	XP_011520941.1:n.4418+1G>A
XM_011522640.1:c.4415+1G>A	XP_011520942.1:n.4415+1G>A
XM_011522641.1:c.4184+1G>A	XP_011520943.1:n.4184+1G>A
NM_000548.4:c.4493+1G>A	NP_000539.2:n.4493+1G>A
NM_001077183.2:c.4292+1G>A	NP_001070651.1:n.4292+1G>A
NM_001114382.2:c.4424+1G>A	NP_001107854.1:n.4424+1G>A
NM_001318827.1:c.4184+1G>A	NP_001305756.1:n.4184+1G>A
NM_001318829.1:c.4148+1G>A	NP_001305758.1:n.4148+1G>A
NM_001318831.1:c.3761+1G>A	NP_001305760.1:n.3761+1G>A
NM_001318832.1:c.4325+1G>A	NP_001305761.1:n.4325+1G>A
NM_001363528.1:c.4295+1G>A	NP_001350457.1:n.4295+1G>A
NM_021055.2:c.4364+1G>A	NP_066399.2:n.4364+1G>A
XM_005255531.4:c.4295+1G>A	XP_005255588.2:n.4295+1G>A
XM_011522636.2:c.4547+1G>A	XP_011520938.1:n.4547+1G>A
XM_011522637.2:c.4544+1G>A	XP_011520939.1:n.4544+1G>A
XM_011522638.2:c.4709+1G>A	XP_011520940.2:n.4709+1G>A
XM_011522639.2:c.4418+1G>A	XP_011520941.1:n.4418+1G>A
XM_011522640.2:c.4415+1G>A	XP_011520942.1:n.4415+1G>A
XM_017023615.1:c.4490+1G>A	XP_016879104.1:n.4490+1G>A
XM_017023616.1:c.4361+1G>A	XP_016879105.1:n.4361+1G>A
XM_017023617.1:c.4457+1G>A	XP_016879106.1:n.4457+1G>A
XM_017023618.1:c.3203+1G>A	XP_016879107.1:n.3203+1G>A
XM_024450413.1:c.4292+1G>A	XP_024306181.1:n.4292+1G>A
NM_000548.5:c.4493+1G>A MANE Select	NP_000539.2:n.4493+1G>A
NM_001370404.1:c.4361+1G>A	NP_001357333.1:n.4361+1G>A
NM_001370405.1:c.4364+1G>A	NP_001357334.1:n.4364+1G>A
NM_001077183.3:c.4292+1G>A	NP_001070651.1:n.4292+1G>A
NM_001114382.3:c.4424+1G>A	NP_001107854.1:n.4424+1G>A
NM_001318827.2:c.4184+1G>A	NP_001305756.1:n.4184+1G>A
NM_001318829.2:c.4148+1G>A	NP_001305758.1:n.4148+1G>A
NM_001318831.2:c.3761+1G>A	NP_001305760.1:n.3761+1G>A
NM_001318832.2:c.4325+1G>A	NP_001305761.1:n.4325+1G>A
NM_001363528.2:c.4295+1G>A	NP_001350457.1:n.4295+1G>A
NM_021055.3:c.4364+1G>A	NP_066399.2:n.4364+1G>A