Canonical Allele Identifier: CA493042763

Gene: TSC2

Linked Data

• ClinVar Variation Id: 851678
• ClinVar RCV Id: RCV001056118 ; RCV004031775
• dbSNP Id: rs2089803859
• MyVariant Identifiers: chr16:g.2129162A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2079161A>G , CM000678.2:g.2079161A>G	GRCh38
NC_000016.9:g.2129162A>G , CM000678.1:g.2129162A>G	GRCh37
NC_000016.8:g.2069163A>G	NCBI36
NG_005895.1:g.34856A>G , LRG_487:g.34856A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*1514A>G	ENSP00000455997.2:n.*1514A>G
ENST00000642206.2:c.3012A>G	ENSP00000495146.2:p.Arg1004=
ENST00000642365.2:c.3093A>G	ENSP00000495459.2:p.Arg1031=
ENST00000644417.2:c.*3545A>G	ENSP00000493912.2:n.*3545A>G
ENST00000646464.2:c.*4018A>G	ENSP00000496610.2:n.*4018A>G
ENST00000219476.9:c.3096A>G MANE Select	ENSP00000219476.3:p.Arg1032=
ENST00000350773.9:c.3096A>G	ENSP00000344383.4:p.Arg1032=
ENST00000401874.7:c.2964A>G	ENSP00000384468.2:p.Arg988=
ENST00000471143.6:c.324A>G	ENSP00000458541.2:n.324A>G
ENST00000568366.6:n.453A>G
ENST00000568454.6:c.2997A>G	ENSP00000454487.1:p.Arg999=
ENST00000642365.1:c.1750A>G
ENST00000642561.1:c.2967A>G	ENSP00000495099.1:p.Arg989=
ENST00000642797.1:c.2967A>G	ENSP00000493846.1:p.Arg989=
ENST00000642936.1:c.2964A>G	ENSP00000494514.1:p.Arg988=
ENST00000643088.1:c.2964A>G	ENSP00000494747.1:p.Arg988=
ENST00000643946.1:c.3096A>G	ENSP00000495927.1:p.Arg1032=
ENST00000644043.1:c.2967A>G	ENSP00000496262.1:p.Arg989=
ENST00000644329.1:c.2964A>G	ENSP00000496611.1:p.Arg988=
ENST00000644335.1:c.2967A>G	ENSP00000496317.1:p.Arg989=
ENST00000644399.1:c.3086A>G
ENST00000644722.1:n.242A>G
ENST00000645024.1:n.1249A>G
ENST00000646388.1:c.3096A>G	ENSP00000495921.1:p.Arg1032=
ENST00000646634.1:n.1980A>G
ENST00000647042.1:n.388A>G
ENST00000219476.7:c.3096A>G	ENSP00000219476.3:p.Arg1032=
ENST00000350773.8:c.3096A>G	ENSP00000344383.4:p.Arg1032=
ENST00000382538.10:c.2820A>G	ENSP00000371978.6:p.Arg940=
ENST00000401874.6:c.2964A>G	ENSP00000384468.2:p.Arg988=
ENST00000439117.6:c.*2263A>G	ENSP00000406980.2:n.*2263A>G
ENST00000439673.6:c.2856A>G	ENSP00000399232.2:p.Arg952=
ENST00000471143.5:c.322A>G
ENST00000483020.5:c.336A>G	ENSP00000460310.1:n.336A>G
ENST00000497886.5:n.923A>G
ENST00000561695.1:n.242A>G
ENST00000568366.5:n.453A>G
ENST00000568454.5:c.2997A>G	ENSP00000454487.1:p.Arg999=
NM_000548.3:c.3096A>G , LRG_487t1:c.3096A>G	NP_000539.2:p.Arg1032=
NM_001077183.1:c.2964A>G	NP_001070651.1:p.Arg988=
NM_001114382.1:c.3096A>G	NP_001107854.1:p.Arg1032=
XM_005255529.3:c.2967A>G	XP_005255586.2:p.Arg989=
XM_005255531.3:c.2967A>G	XP_005255588.2:p.Arg989=
XM_011522636.1:c.3096A>G	XP_011520938.1:p.Arg1032=
XM_011522637.1:c.3093A>G	XP_011520939.1:p.Arg1031=
XM_011522638.1:c.2985A>G	XP_011520940.1:p.Arg995=
XM_011522639.1:c.2967A>G	XP_011520941.1:p.Arg989=
XM_011522640.1:c.2964A>G	XP_011520942.1:p.Arg988=
XM_011522641.1:c.2856A>G	XP_011520943.1:p.Arg952=
NM_000548.4:c.3096A>G	NP_000539.2:p.Arg1032=
NM_001077183.2:c.2964A>G	NP_001070651.1:p.Arg988=
NM_001114382.2:c.3096A>G	NP_001107854.1:p.Arg1032=
NM_001318827.1:c.2856A>G	NP_001305756.1:p.Arg952=
NM_001318829.1:c.2820A>G	NP_001305758.1:p.Arg940=
NM_001318831.1:c.2364A>G	NP_001305760.1:p.Arg788=
NM_001318832.1:c.2997A>G	NP_001305761.1:p.Arg999=
NM_001363528.1:c.2967A>G	NP_001350457.1:p.Arg989=
NM_021055.2:c.2967A>G	NP_066399.2:p.Arg989=
XM_005255531.4:c.2967A>G	XP_005255588.2:p.Arg989=
XM_011522636.2:c.3096A>G	XP_011520938.1:p.Arg1032=
XM_011522637.2:c.3093A>G	XP_011520939.1:p.Arg1031=
XM_011522638.2:c.3258A>G	XP_011520940.2:p.Arg1086=
XM_011522639.2:c.2967A>G	XP_011520941.1:p.Arg989=
XM_011522640.2:c.2964A>G	XP_011520942.1:p.Arg988=
XM_017023615.1:c.3093A>G	XP_016879104.1:p.Arg1031=
XM_017023616.1:c.2964A>G	XP_016879105.1:p.Arg988=
XM_017023617.1:c.3129A>G	XP_016879106.1:p.Arg1043=
XM_017023618.1:c.1752A>G	XP_016879107.1:p.Arg584=
XM_024450413.1:c.2964A>G	XP_024306181.1:p.Arg988=
NM_000548.5:c.3096A>G MANE Select	NP_000539.2:p.Arg1032=
NM_001370404.1:c.2964A>G	NP_001357333.1:p.Arg988=
NM_001370405.1:c.2967A>G	NP_001357334.1:p.Arg989=
NM_001077183.3:c.2964A>G	NP_001070651.1:p.Arg988=
NM_001114382.3:c.3096A>G	NP_001107854.1:p.Arg1032=
NM_001318827.2:c.2856A>G	NP_001305756.1:p.Arg952=
NM_001318829.2:c.2820A>G	NP_001305758.1:p.Arg940=
NM_001318831.2:c.2364A>G	NP_001305760.1:p.Arg788=
NM_001318832.2:c.2997A>G	NP_001305761.1:p.Arg999=
NM_001363528.2:c.2967A>G	NP_001350457.1:p.Arg989=
NM_021055.3:c.2967A>G	NP_066399.2:p.Arg989=