Canonical Allele Identifier: CA493043334

Gene: TSC2

Linked Data

• MyVariant Identifiers: chr16:g.2134645A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2084644A>G , CM000678.2:g.2084644A>G	GRCh38
NC_000016.9:g.2134645A>G , CM000678.1:g.2134645A>G	GRCh37
NC_000016.8:g.2074646A>G	NCBI36
NG_005895.1:g.40339A>G , LRG_487:g.40339A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*2771A>G	ENSP00000455997.2:n.*2771A>G
ENST00000642206.2:c.4269A>G	ENSP00000495146.2:p.Arg1423=
ENST00000642365.2:c.4419A>G	ENSP00000495459.2:p.Arg1473=
ENST00000644417.2:c.*4802A>G	ENSP00000493912.2:n.*4802A>G
ENST00000646464.2:c.*7171A>G	ENSP00000496610.2:n.*7171A>G
ENST00000219476.9:c.4422A>G MANE Select	ENSP00000219476.3:p.Arg1474=
ENST00000350773.9:c.4353A>G	ENSP00000344383.4:p.Arg1451=
ENST00000401874.7:c.4221A>G	ENSP00000384468.2:p.Arg1407=
ENST00000568454.6:c.4254A>G	ENSP00000454487.1:p.Arg1418=
ENST00000569110.2:c.658A>G
ENST00000569930.2:n.2304A>G
ENST00000642365.1:c.3076A>G
ENST00000642561.1:c.4293A>G	ENSP00000495099.1:p.Arg1431=
ENST00000642728.1:n.604A>G
ENST00000642797.1:c.4224A>G	ENSP00000493846.1:p.Arg1408=
ENST00000642936.1:c.4290A>G	ENSP00000494514.1:p.Arg1430=
ENST00000643088.1:c.4221A>G	ENSP00000494747.1:p.Arg1407=
ENST00000643177.1:n.436A>G
ENST00000643426.1:n.2070A>G
ENST00000643946.1:c.4353A>G	ENSP00000495927.1:p.Arg1451=
ENST00000644043.1:c.4293A>G	ENSP00000496262.1:p.Arg1431=
ENST00000644329.1:c.4221A>G	ENSP00000496611.1:p.Arg1407=
ENST00000644335.1:c.4224A>G	ENSP00000496317.1:p.Arg1408=
ENST00000644399.1:c.4343A>G
ENST00000645024.1:n.2506A>G
ENST00000646388.1:c.4422A>G	ENSP00000495921.1:p.Arg1474=
ENST00000646634.1:n.3237A>G
ENST00000646674.1:n.1674A>G
ENST00000647042.1:n.1645A>G
ENST00000647180.1:n.1535A>G
ENST00000219476.7:c.4422A>G	ENSP00000219476.3:p.Arg1474=
ENST00000350773.8:c.4353A>G	ENSP00000344383.4:p.Arg1451=
ENST00000382538.10:c.4077A>G	ENSP00000371978.6:p.Arg1359=
ENST00000401874.6:c.4221A>G	ENSP00000384468.2:p.Arg1407=
ENST00000439117.6:c.*3589A>G	ENSP00000406980.2:n.*3589A>G
ENST00000439673.6:c.4113A>G	ENSP00000399232.2:p.Arg1371=
ENST00000497886.5:n.2180A>G
ENST00000568454.5:c.4254A>G	ENSP00000454487.1:p.Arg1418=
ENST00000569110.1:c.604A>G
ENST00000569930.1:n.1537A>G
NM_000548.3:c.4422A>G , LRG_487t1:c.4422A>G	NP_000539.2:p.Arg1474=
NM_001077183.1:c.4221A>G	NP_001070651.1:p.Arg1407=
NM_001114382.1:c.4353A>G	NP_001107854.1:p.Arg1451=
XM_005255529.3:c.4293A>G	XP_005255586.2:p.Arg1431=
XM_005255531.3:c.4224A>G	XP_005255588.2:p.Arg1408=
XM_011522636.1:c.4476A>G	XP_011520938.1:p.Arg1492=
XM_011522637.1:c.4473A>G	XP_011520939.1:p.Arg1491=
XM_011522638.1:c.4365A>G	XP_011520940.1:p.Arg1455=
XM_011522639.1:c.4347A>G	XP_011520941.1:p.Arg1449=
XM_011522640.1:c.4344A>G	XP_011520942.1:p.Arg1448=
XM_011522641.1:c.4113A>G	XP_011520943.1:p.Arg1371=
NM_000548.4:c.4422A>G	NP_000539.2:p.Arg1474=
NM_001077183.2:c.4221A>G	NP_001070651.1:p.Arg1407=
NM_001114382.2:c.4353A>G	NP_001107854.1:p.Arg1451=
NM_001318827.1:c.4113A>G	NP_001305756.1:p.Arg1371=
NM_001318829.1:c.4077A>G	NP_001305758.1:p.Arg1359=
NM_001318831.1:c.3690A>G	NP_001305760.1:p.Arg1230=
NM_001318832.1:c.4254A>G	NP_001305761.1:p.Arg1418=
NM_001363528.1:c.4224A>G	NP_001350457.1:p.Arg1408=
NM_021055.2:c.4293A>G	NP_066399.2:p.Arg1431=
XM_005255531.4:c.4224A>G	XP_005255588.2:p.Arg1408=
XM_011522636.2:c.4476A>G	XP_011520938.1:p.Arg1492=
XM_011522637.2:c.4473A>G	XP_011520939.1:p.Arg1491=
XM_011522638.2:c.4638A>G	XP_011520940.2:p.Arg1546=
XM_011522639.2:c.4347A>G	XP_011520941.1:p.Arg1449=
XM_011522640.2:c.4344A>G	XP_011520942.1:p.Arg1448=
XM_017023615.1:c.4419A>G	XP_016879104.1:p.Arg1473=
XM_017023616.1:c.4290A>G	XP_016879105.1:p.Arg1430=
XM_017023617.1:c.4386A>G	XP_016879106.1:p.Arg1462=
XM_017023618.1:c.3132A>G	XP_016879107.1:p.Arg1044=
XM_024450413.1:c.4221A>G	XP_024306181.1:p.Arg1407=
NM_000548.5:c.4422A>G MANE Select	NP_000539.2:p.Arg1474=
NM_001370404.1:c.4290A>G	NP_001357333.1:p.Arg1430=
NM_001370405.1:c.4293A>G	NP_001357334.1:p.Arg1431=
NM_001077183.3:c.4221A>G	NP_001070651.1:p.Arg1407=
NM_001114382.3:c.4353A>G	NP_001107854.1:p.Arg1451=
NM_001318827.2:c.4113A>G	NP_001305756.1:p.Arg1371=
NM_001318829.2:c.4077A>G	NP_001305758.1:p.Arg1359=
NM_001318831.2:c.3690A>G	NP_001305760.1:p.Arg1230=
NM_001318832.2:c.4254A>G	NP_001305761.1:p.Arg1418=
NM_001363528.2:c.4224A>G	NP_001350457.1:p.Arg1408=
NM_021055.3:c.4293A>G	NP_066399.2:p.Arg1431=