Canonical Allele Identifier: CA394314388

Gene: TSC2

Linked Data

• dbSNP Id: rs2151630518
• MyVariant Identifiers: chr16:g.2138280C>A (hg19) ; chr16:g.2088279C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2088279C>A , CM000678.2:g.2088279C>A	GRCh38
NC_000016.9:g.2138280C>A , CM000678.1:g.2138280C>A	GRCh37
NC_000016.8:g.2078281C>A	NCBI36
NG_005895.1:g.43974C>A , LRG_487:g.43974C>A
NG_008617.1:g.54942G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*3562C>A	ENSP00000455997.2:n.*3562C>A
ENST00000642206.2:c.5060C>A	ENSP00000495146.2:p.Ser1687Tyr
ENST00000642365.2:c.5210C>A	ENSP00000495459.2:p.Ser1737Tyr
ENST00000644417.2:c.*5726C>A	ENSP00000493912.2:n.*5726C>A
ENST00000646464.2:c.*7962C>A	ENSP00000496610.2:n.*7962C>A
ENST00000219476.9:c.5213C>A MANE Select	ENSP00000219476.3:p.Ser1738Tyr
ENST00000350773.9:c.5144C>A	ENSP00000344383.4:p.Ser1715Tyr
ENST00000401874.7:c.5012C>A	ENSP00000384468.2:p.Ser1671Tyr
ENST00000568454.6:c.5045C>A	ENSP00000454487.1:p.Ser1682Tyr
ENST00000569110.2:c.1436C>A
ENST00000569930.2:n.3095C>A
ENST00000642365.1:c.3867C>A
ENST00000642561.1:c.5072C>A	ENSP00000495099.1:p.Ser1691Tyr
ENST00000642791.1:n.810C>A
ENST00000642797.1:c.5015C>A	ENSP00000493846.1:p.Ser1672Tyr
ENST00000642936.1:c.5081C>A	ENSP00000494514.1:p.Ser1694Tyr
ENST00000643088.1:c.5006C>A	ENSP00000494747.1:p.Ser1669Tyr
ENST00000643426.1:n.2861C>A
ENST00000643946.1:c.5138C>A	ENSP00000495927.1:p.Ser1713Tyr
ENST00000644043.1:c.5084C>A	ENSP00000496262.1:p.Ser1695Tyr
ENST00000644329.1:c.5099C>A	ENSP00000496611.1:p.Ser1700Tyr
ENST00000644335.1:c.5009C>A	ENSP00000496317.1:p.Ser1670Tyr
ENST00000644399.1:c.5134C>A
ENST00000645024.1:n.3297C>A
ENST00000646388.1:c.5207C>A	ENSP00000495921.1:p.Ser1736Tyr
ENST00000646634.1:n.4028C>A
ENST00000646674.1:n.2465C>A
ENST00000647042.1:n.2436C>A
ENST00000647180.1:n.2326C>A
ENST00000219476.7:c.5213C>A	ENSP00000219476.3:p.Ser1738Tyr
ENST00000350773.8:c.5144C>A	ENSP00000344383.4:p.Ser1715Tyr
ENST00000382538.10:c.4868C>A	ENSP00000371978.6:p.Ser1623Tyr
ENST00000401874.6:c.5012C>A	ENSP00000384468.2:p.Ser1671Tyr
ENST00000439117.6:c.*4380C>A	ENSP00000406980.2:n.*4380C>A
ENST00000439673.6:c.4904C>A	ENSP00000399232.2:p.Ser1635Tyr
ENST00000497886.5:n.2936C>A
ENST00000568454.5:c.5045C>A	ENSP00000454487.1:p.Ser1682Tyr
ENST00000569110.1:c.1395C>A
ENST00000569930.1:n.2328C>A
NM_000548.3:c.5213C>A , LRG_487t1:c.5213C>A	NP_000539.2:p.Ser1738Tyr
NM_001077183.1:c.5012C>A	NP_001070651.1:p.Ser1671Tyr
NM_001114382.1:c.5144C>A	NP_001107854.1:p.Ser1715Tyr
XM_005255529.3:c.5084C>A	XP_005255586.2:p.Ser1695Tyr
XM_005255531.3:c.5015C>A	XP_005255588.2:p.Ser1672Tyr
XM_011522636.1:c.5267C>A	XP_011520938.1:p.Ser1756Tyr
XM_011522637.1:c.5264C>A	XP_011520939.1:p.Ser1755Tyr
XM_011522638.1:c.5156C>A	XP_011520940.1:p.Ser1719Tyr
XM_011522639.1:c.5138C>A	XP_011520941.1:p.Ser1713Tyr
XM_011522640.1:c.5135C>A	XP_011520942.1:p.Ser1712Tyr
XM_011522641.1:c.4904C>A	XP_011520943.1:p.Ser1635Tyr
NM_000548.4:c.5213C>A	NP_000539.2:p.Ser1738Tyr
NM_001077183.2:c.5012C>A	NP_001070651.1:p.Ser1671Tyr
NM_001114382.2:c.5144C>A	NP_001107854.1:p.Ser1715Tyr
NM_001318827.1:c.4904C>A	NP_001305756.1:p.Ser1635Tyr
NM_001318829.1:c.4868C>A	NP_001305758.1:p.Ser1623Tyr
NM_001318831.1:c.4481C>A	NP_001305760.1:p.Ser1494Tyr
NM_001318832.1:c.5045C>A	NP_001305761.1:p.Ser1682Tyr
NM_001363528.1:c.5015C>A	NP_001350457.1:p.Ser1672Tyr
NM_021055.2:c.5084C>A	NP_066399.2:p.Ser1695Tyr
XM_005255531.4:c.5015C>A	XP_005255588.2:p.Ser1672Tyr
XM_011522636.2:c.5267C>A	XP_011520938.1:p.Ser1756Tyr
XM_011522637.2:c.5264C>A	XP_011520939.1:p.Ser1755Tyr
XM_011522638.2:c.5429C>A	XP_011520940.2:p.Ser1810Tyr
XM_011522639.2:c.5138C>A	XP_011520941.1:p.Ser1713Tyr
XM_011522640.2:c.5135C>A	XP_011520942.1:p.Ser1712Tyr
XM_017023615.1:c.5210C>A	XP_016879104.1:p.Ser1737Tyr
XM_017023616.1:c.5081C>A	XP_016879105.1:p.Ser1694Tyr
XM_017023617.1:c.5177C>A	XP_016879106.1:p.Ser1726Tyr
XM_017023618.1:c.3923C>A	XP_016879107.1:p.Ser1308Tyr
XM_024450413.1:c.5099C>A	XP_024306181.1:p.Ser1700Tyr
NM_000548.5:c.5213C>A MANE Select	NP_000539.2:p.Ser1738Tyr
NM_001370404.1:c.5081C>A	NP_001357333.1:p.Ser1694Tyr
NM_001370405.1:c.5072C>A	NP_001357334.1:p.Ser1691Tyr
NM_001077183.3:c.5012C>A	NP_001070651.1:p.Ser1671Tyr
NM_001114382.3:c.5144C>A	NP_001107854.1:p.Ser1715Tyr
NM_001318827.2:c.4904C>A	NP_001305756.1:p.Ser1635Tyr
NM_001318829.2:c.4868C>A	NP_001305758.1:p.Ser1623Tyr
NM_001318831.2:c.4481C>A	NP_001305760.1:p.Ser1494Tyr
NM_001318832.2:c.5045C>A	NP_001305761.1:p.Ser1682Tyr
NM_001363528.2:c.5015C>A	NP_001350457.1:p.Ser1672Tyr
NM_021055.3:c.5084C>A	NP_066399.2:p.Ser1695Tyr