Canonical Allele Identifier: CA493042965

Gene: TSC2

Linked Data

• ClinVar Variation Id: 486704
• ClinVar RCV Id: RCV000561556 ; RCV001434679
• dbSNP Id: rs1555512292
• MyVariant Identifiers: chr16:g.2131597G>A (hg19) ; chr16:g.2081596G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2081596G>A , CM000678.2:g.2081596G>A	GRCh38
NC_000016.9:g.2131597G>A , CM000678.1:g.2131597G>A	GRCh37
NC_000016.8:g.2071598G>A	NCBI36
NG_005895.1:g.37291G>A , LRG_487:g.37291G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*2030G>A	ENSP00000455997.2:n.*2030G>A
ENST00000642206.2:c.3528G>A	ENSP00000495146.2:p.Gly1176=
ENST00000642365.2:c.3609G>A	ENSP00000495459.2:p.Gly1203=
ENST00000644417.2:c.*4061G>A	ENSP00000493912.2:n.*4061G>A
ENST00000646464.2:c.*4534G>A	ENSP00000496610.2:n.*4534G>A
ENST00000219476.9:c.3612G>A MANE Select	ENSP00000219476.3:p.Gly1204=
ENST00000350773.9:c.3612G>A	ENSP00000344383.4:p.Gly1204=
ENST00000401874.7:c.3480G>A	ENSP00000384468.2:p.Gly1160=
ENST00000568454.6:c.3513G>A	ENSP00000454487.1:p.Gly1171=
ENST00000642365.1:c.2266G>A
ENST00000642561.1:c.3483G>A	ENSP00000495099.1:p.Gly1161=
ENST00000642797.1:c.3483G>A	ENSP00000493846.1:p.Gly1161=
ENST00000642936.1:c.3480G>A	ENSP00000494514.1:p.Gly1160=
ENST00000643088.1:c.3480G>A	ENSP00000494747.1:p.Gly1160=
ENST00000643426.1:n.1260G>A
ENST00000643533.1:n.122G>A
ENST00000643946.1:c.3612G>A	ENSP00000495927.1:p.Gly1204=
ENST00000644043.1:c.3483G>A	ENSP00000496262.1:p.Gly1161=
ENST00000644329.1:c.3480G>A	ENSP00000496611.1:p.Gly1160=
ENST00000644335.1:c.3483G>A	ENSP00000496317.1:p.Gly1161=
ENST00000644399.1:c.3602G>A
ENST00000644722.1:n.758G>A
ENST00000645024.1:n.1765G>A
ENST00000646388.1:c.3612G>A	ENSP00000495921.1:p.Gly1204=
ENST00000646634.1:n.2496G>A
ENST00000646674.1:n.227G>A
ENST00000647042.1:n.904G>A
ENST00000647180.1:n.92G>A
ENST00000219476.7:c.3612G>A	ENSP00000219476.3:p.Gly1204=
ENST00000350773.8:c.3612G>A	ENSP00000344383.4:p.Gly1204=
ENST00000382538.10:c.3336G>A	ENSP00000371978.6:p.Gly1112=
ENST00000401874.6:c.3480G>A	ENSP00000384468.2:p.Gly1160=
ENST00000439117.6:c.*2779G>A	ENSP00000406980.2:n.*2779G>A
ENST00000439673.6:c.3372G>A	ENSP00000399232.2:p.Gly1124=
ENST00000497886.5:n.1439G>A
ENST00000568454.5:c.3513G>A	ENSP00000454487.1:p.Gly1171=
NM_000548.3:c.3612G>A , LRG_487t1:c.3612G>A	NP_000539.2:p.Gly1204=
NM_001077183.1:c.3480G>A	NP_001070651.1:p.Gly1160=
NM_001114382.1:c.3612G>A	NP_001107854.1:p.Gly1204=
XM_005255529.3:c.3483G>A	XP_005255586.2:p.Gly1161=
XM_005255531.3:c.3483G>A	XP_005255588.2:p.Gly1161=
XM_011522636.1:c.3612G>A	XP_011520938.1:p.Gly1204=
XM_011522637.1:c.3609G>A	XP_011520939.1:p.Gly1203=
XM_011522638.1:c.3501G>A	XP_011520940.1:p.Gly1167=
XM_011522639.1:c.3483G>A	XP_011520941.1:p.Gly1161=
XM_011522640.1:c.3480G>A	XP_011520942.1:p.Gly1160=
XM_011522641.1:c.3372G>A	XP_011520943.1:p.Gly1124=
NM_000548.4:c.3612G>A	NP_000539.2:p.Gly1204=
NM_001077183.2:c.3480G>A	NP_001070651.1:p.Gly1160=
NM_001114382.2:c.3612G>A	NP_001107854.1:p.Gly1204=
NM_001318827.1:c.3372G>A	NP_001305756.1:p.Gly1124=
NM_001318829.1:c.3336G>A	NP_001305758.1:p.Gly1112=
NM_001318831.1:c.2880G>A	NP_001305760.1:p.Gly960=
NM_001318832.1:c.3513G>A	NP_001305761.1:p.Gly1171=
NM_001363528.1:c.3483G>A	NP_001350457.1:p.Gly1161=
NM_021055.2:c.3483G>A	NP_066399.2:p.Gly1161=
XM_005255531.4:c.3483G>A	XP_005255588.2:p.Gly1161=
XM_011522636.2:c.3612G>A	XP_011520938.1:p.Gly1204=
XM_011522637.2:c.3609G>A	XP_011520939.1:p.Gly1203=
XM_011522638.2:c.3774G>A	XP_011520940.2:p.Gly1258=
XM_011522639.2:c.3483G>A	XP_011520941.1:p.Gly1161=
XM_011522640.2:c.3480G>A	XP_011520942.1:p.Gly1160=
XM_017023615.1:c.3609G>A	XP_016879104.1:p.Gly1203=
XM_017023616.1:c.3480G>A	XP_016879105.1:p.Gly1160=
XM_017023617.1:c.3645G>A	XP_016879106.1:p.Gly1215=
XM_017023618.1:c.2268G>A	XP_016879107.1:p.Gly756=
XM_024450413.1:c.3480G>A	XP_024306181.1:p.Gly1160=
NM_000548.5:c.3612G>A MANE Select	NP_000539.2:p.Gly1204=
NM_001370404.1:c.3480G>A	NP_001357333.1:p.Gly1160=
NM_001370405.1:c.3483G>A	NP_001357334.1:p.Gly1161=
NM_001077183.3:c.3480G>A	NP_001070651.1:p.Gly1160=
NM_001114382.3:c.3612G>A	NP_001107854.1:p.Gly1204=
NM_001318827.2:c.3372G>A	NP_001305756.1:p.Gly1124=
NM_001318829.2:c.3336G>A	NP_001305758.1:p.Gly1112=
NM_001318831.2:c.2880G>A	NP_001305760.1:p.Gly960=
NM_001318832.2:c.3513G>A	NP_001305761.1:p.Gly1171=
NM_001363528.2:c.3483G>A	NP_001350457.1:p.Gly1161=
NM_021055.3:c.3483G>A	NP_066399.2:p.Gly1161=