Canonical Allele Identifier: CA020509

Gene: TSC2

Linked Data

• ClinVar Variation Id: 49490
• ClinVar RCV Id: RCV000042750 ; RCV001852889 ; RCV003441731
• dbSNP Id: rs45517344
• MyVariant Identifiers: chr16:g.2134712C>A (hg19) ; chr16:g.2084711C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2084711C>A , CM000678.2:g.2084711C>A	GRCh38
NC_000016.9:g.2134712C>A , CM000678.1:g.2134712C>A	GRCh37
NC_000016.8:g.2074713C>A	NCBI36
NG_005895.1:g.40406C>A , LRG_487:g.40406C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*2838C>A	ENSP00000455997.2:n.*2838C>A
ENST00000642206.2:c.4336C>A	ENSP00000495146.2:p.Pro1446Thr
ENST00000642365.2:c.4486C>A	ENSP00000495459.2:p.Pro1496Thr
ENST00000644417.2:c.*4869C>A	ENSP00000493912.2:n.*4869C>A
ENST00000646464.2:c.*7238C>A	ENSP00000496610.2:n.*7238C>A
ENST00000219476.9:c.4489C>A MANE Select	ENSP00000219476.3:p.Pro1497Thr
ENST00000350773.9:c.4420C>A	ENSP00000344383.4:p.Pro1474Thr
ENST00000401874.7:c.4288C>A	ENSP00000384468.2:p.Pro1430Thr
ENST00000568454.6:c.4321C>A	ENSP00000454487.1:p.Pro1441Thr
ENST00000569110.2:c.716+9C>A
ENST00000569930.2:n.2371C>A
ENST00000642365.1:c.3143C>A
ENST00000642561.1:c.4360C>A	ENSP00000495099.1:p.Pro1454Thr
ENST00000642728.1:n.671C>A
ENST00000642797.1:c.4291C>A	ENSP00000493846.1:p.Pro1431Thr
ENST00000642936.1:c.4357C>A	ENSP00000494514.1:p.Pro1453Thr
ENST00000643088.1:c.4288C>A	ENSP00000494747.1:p.Pro1430Thr
ENST00000643177.1:n.503C>A
ENST00000643426.1:n.2137C>A
ENST00000643946.1:c.4420C>A	ENSP00000495927.1:p.Pro1474Thr
ENST00000644043.1:c.4360C>A	ENSP00000496262.1:p.Pro1454Thr
ENST00000644329.1:c.4288C>A	ENSP00000496611.1:p.Pro1430Thr
ENST00000644335.1:c.4291C>A	ENSP00000496317.1:p.Pro1431Thr
ENST00000644399.1:c.4410C>A
ENST00000645024.1:n.2573C>A
ENST00000646388.1:c.4489C>A	ENSP00000495921.1:p.Pro1497Thr
ENST00000646634.1:n.3304C>A
ENST00000646674.1:n.1741C>A
ENST00000647042.1:n.1712C>A
ENST00000647180.1:n.1602C>A
ENST00000219476.7:c.4489C>A	ENSP00000219476.3:p.Pro1497Thr
ENST00000350773.8:c.4420C>A	ENSP00000344383.4:p.Pro1474Thr
ENST00000382538.10:c.4144C>A	ENSP00000371978.6:p.Pro1382Thr
ENST00000401874.6:c.4288C>A	ENSP00000384468.2:p.Pro1430Thr
ENST00000439117.6:c.*3656C>A	ENSP00000406980.2:n.*3656C>A
ENST00000439673.6:c.4180C>A	ENSP00000399232.2:p.Pro1394Thr
ENST00000497886.5:n.2247C>A
ENST00000568454.5:c.4321C>A	ENSP00000454487.1:p.Pro1441Thr
ENST00000569110.1:c.671C>A
ENST00000569930.1:n.1604C>A
NM_000548.3:c.4489C>A , LRG_487t1:c.4489C>A	NP_000539.2:p.Pro1497Thr
NM_001077183.1:c.4288C>A	NP_001070651.1:p.Pro1430Thr
NM_001114382.1:c.4420C>A	NP_001107854.1:p.Pro1474Thr
XM_005255529.3:c.4360C>A	XP_005255586.2:p.Pro1454Thr
XM_005255531.3:c.4291C>A	XP_005255588.2:p.Pro1431Thr
XM_011522636.1:c.4543C>A	XP_011520938.1:p.Pro1515Thr
XM_011522637.1:c.4540C>A	XP_011520939.1:p.Pro1514Thr
XM_011522638.1:c.4432C>A	XP_011520940.1:p.Pro1478Thr
XM_011522639.1:c.4414C>A	XP_011520941.1:p.Pro1472Thr
XM_011522640.1:c.4411C>A	XP_011520942.1:p.Pro1471Thr
XM_011522641.1:c.4180C>A	XP_011520943.1:p.Pro1394Thr
NM_000548.4:c.4489C>A	NP_000539.2:p.Pro1497Thr
NM_001077183.2:c.4288C>A	NP_001070651.1:p.Pro1430Thr
NM_001114382.2:c.4420C>A	NP_001107854.1:p.Pro1474Thr
NM_001318827.1:c.4180C>A	NP_001305756.1:p.Pro1394Thr
NM_001318829.1:c.4144C>A	NP_001305758.1:p.Pro1382Thr
NM_001318831.1:c.3757C>A	NP_001305760.1:p.Pro1253Thr
NM_001318832.1:c.4321C>A	NP_001305761.1:p.Pro1441Thr
NM_001363528.1:c.4291C>A	NP_001350457.1:p.Pro1431Thr
NM_021055.2:c.4360C>A	NP_066399.2:p.Pro1454Thr
XM_005255531.4:c.4291C>A	XP_005255588.2:p.Pro1431Thr
XM_011522636.2:c.4543C>A	XP_011520938.1:p.Pro1515Thr
XM_011522637.2:c.4540C>A	XP_011520939.1:p.Pro1514Thr
XM_011522638.2:c.4705C>A	XP_011520940.2:p.Pro1569Thr
XM_011522639.2:c.4414C>A	XP_011520941.1:p.Pro1472Thr
XM_011522640.2:c.4411C>A	XP_011520942.1:p.Pro1471Thr
XM_017023615.1:c.4486C>A	XP_016879104.1:p.Pro1496Thr
XM_017023616.1:c.4357C>A	XP_016879105.1:p.Pro1453Thr
XM_017023617.1:c.4453C>A	XP_016879106.1:p.Pro1485Thr
XM_017023618.1:c.3199C>A	XP_016879107.1:p.Pro1067Thr
XM_024450413.1:c.4288C>A	XP_024306181.1:p.Pro1430Thr
NM_000548.5:c.4489C>A MANE Select	NP_000539.2:p.Pro1497Thr
NM_001370404.1:c.4357C>A	NP_001357333.1:p.Pro1453Thr
NM_001370405.1:c.4360C>A	NP_001357334.1:p.Pro1454Thr
NM_001077183.3:c.4288C>A	NP_001070651.1:p.Pro1430Thr
NM_001114382.3:c.4420C>A	NP_001107854.1:p.Pro1474Thr
NM_001318827.2:c.4180C>A	NP_001305756.1:p.Pro1394Thr
NM_001318829.2:c.4144C>A	NP_001305758.1:p.Pro1382Thr
NM_001318831.2:c.3757C>A	NP_001305760.1:p.Pro1253Thr
NM_001318832.2:c.4321C>A	NP_001305761.1:p.Pro1441Thr
NM_001363528.2:c.4291C>A	NP_001350457.1:p.Pro1431Thr
NM_021055.3:c.4360C>A	NP_066399.2:p.Pro1454Thr