Canonical Allele Identifier: CA021852

Gene: TSC2

Linked Data

• ClinVar Variation Id: 49351
• ClinVar RCV Id: RCV000042611 ; RCV000506833 ; RCV000793317
• dbSNP Id: rs45517396
• MyVariant Identifiers: chr16:g.2138120C>T (hg19) ; chr16:g.2088119C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2088119C>T , CM000678.2:g.2088119C>T	GRCh38
NC_000016.9:g.2138120C>T , CM000678.1:g.2138120C>T	GRCh37
NC_000016.8:g.2078121C>T	NCBI36
NG_005895.1:g.43814C>T , LRG_487:g.43814C>T
NG_008617.1:g.55102G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*3489C>T	ENSP00000455997.2:n.*3489C>T
ENST00000642206.2:c.4987C>T	ENSP00000495146.2:p.Gln1663Ter
ENST00000642365.2:c.5137C>T	ENSP00000495459.2:p.Gln1713Ter
ENST00000644417.2:c.*5653C>T	ENSP00000493912.2:n.*5653C>T
ENST00000646464.2:c.*7889C>T	ENSP00000496610.2:n.*7889C>T
ENST00000219476.9:c.5140C>T MANE Select	ENSP00000219476.3:p.Gln1714Ter
ENST00000350773.9:c.5071C>T	ENSP00000344383.4:p.Gln1691Ter
ENST00000401874.7:c.4939C>T	ENSP00000384468.2:p.Gln1647Ter
ENST00000568454.6:c.4972C>T	ENSP00000454487.1:p.Gln1658Ter
ENST00000569110.2:c.1363C>T
ENST00000569930.2:n.3022C>T
ENST00000642365.1:c.3794C>T
ENST00000642561.1:c.5011C>T	ENSP00000495099.1:p.Gln1671Ter
ENST00000642791.1:n.737C>T
ENST00000642797.1:c.4942C>T	ENSP00000493846.1:p.Gln1648Ter
ENST00000642936.1:c.5008C>T	ENSP00000494514.1:p.Gln1670Ter
ENST00000643088.1:c.4933C>T	ENSP00000494747.1:p.Gln1645Ter
ENST00000643426.1:n.2788C>T
ENST00000643946.1:c.5065C>T	ENSP00000495927.1:p.Gln1689Ter
ENST00000644043.1:c.5011C>T	ENSP00000496262.1:p.Gln1671Ter
ENST00000644329.1:c.4939C>T	ENSP00000496611.1:p.Gln1647Ter
ENST00000644335.1:c.4936C>T	ENSP00000496317.1:p.Gln1646Ter
ENST00000644399.1:c.5061C>T
ENST00000645024.1:n.3224C>T
ENST00000646388.1:c.5134C>T	ENSP00000495921.1:p.Gln1712Ter
ENST00000646634.1:n.3955C>T
ENST00000646674.1:n.2392C>T
ENST00000647042.1:n.2363C>T
ENST00000647180.1:n.2253C>T
ENST00000219476.7:c.5140C>T	ENSP00000219476.3:p.Gln1714Ter
ENST00000350773.8:c.5071C>T	ENSP00000344383.4:p.Gln1691Ter
ENST00000382538.10:c.4795C>T	ENSP00000371978.6:p.Gln1599Ter
ENST00000401874.6:c.4939C>T	ENSP00000384468.2:p.Gln1647Ter
ENST00000439117.6:c.*4307C>T	ENSP00000406980.2:n.*4307C>T
ENST00000439673.6:c.4831C>T	ENSP00000399232.2:p.Gln1611Ter
ENST00000497886.5:n.2863C>T
ENST00000568454.5:c.4972C>T	ENSP00000454487.1:p.Gln1658Ter
ENST00000569110.1:c.1322C>T
ENST00000569930.1:n.2255C>T
NM_000548.3:c.5140C>T , LRG_487t1:c.5140C>T	NP_000539.2:p.Gln1714Ter
NM_001077183.1:c.4939C>T	NP_001070651.1:p.Gln1647Ter
NM_001114382.1:c.5071C>T	NP_001107854.1:p.Gln1691Ter
XM_005255529.3:c.5011C>T	XP_005255586.2:p.Gln1671Ter
XM_005255531.3:c.4942C>T	XP_005255588.2:p.Gln1648Ter
XM_011522636.1:c.5194C>T	XP_011520938.1:p.Gln1732Ter
XM_011522637.1:c.5191C>T	XP_011520939.1:p.Gln1731Ter
XM_011522638.1:c.5083C>T	XP_011520940.1:p.Gln1695Ter
XM_011522639.1:c.5065C>T	XP_011520941.1:p.Gln1689Ter
XM_011522640.1:c.5062C>T	XP_011520942.1:p.Gln1688Ter
XM_011522641.1:c.4831C>T	XP_011520943.1:p.Gln1611Ter
NM_000548.4:c.5140C>T	NP_000539.2:p.Gln1714Ter
NM_001077183.2:c.4939C>T	NP_001070651.1:p.Gln1647Ter
NM_001114382.2:c.5071C>T	NP_001107854.1:p.Gln1691Ter
NM_001318827.1:c.4831C>T	NP_001305756.1:p.Gln1611Ter
NM_001318829.1:c.4795C>T	NP_001305758.1:p.Gln1599Ter
NM_001318831.1:c.4408C>T	NP_001305760.1:p.Gln1470Ter
NM_001318832.1:c.4972C>T	NP_001305761.1:p.Gln1658Ter
NM_001363528.1:c.4942C>T	NP_001350457.1:p.Gln1648Ter
NM_021055.2:c.5011C>T	NP_066399.2:p.Gln1671Ter
XM_005255531.4:c.4942C>T	XP_005255588.2:p.Gln1648Ter
XM_011522636.2:c.5194C>T	XP_011520938.1:p.Gln1732Ter
XM_011522637.2:c.5191C>T	XP_011520939.1:p.Gln1731Ter
XM_011522638.2:c.5356C>T	XP_011520940.2:p.Gln1786Ter
XM_011522639.2:c.5065C>T	XP_011520941.1:p.Gln1689Ter
XM_011522640.2:c.5062C>T	XP_011520942.1:p.Gln1688Ter
XM_017023615.1:c.5137C>T	XP_016879104.1:p.Gln1713Ter
XM_017023616.1:c.5008C>T	XP_016879105.1:p.Gln1670Ter
XM_017023617.1:c.5104C>T	XP_016879106.1:p.Gln1702Ter
XM_017023618.1:c.3850C>T	XP_016879107.1:p.Gln1284Ter
XM_024450413.1:c.4939C>T	XP_024306181.1:p.Gln1647Ter
NM_000548.5:c.5140C>T MANE Select	NP_000539.2:p.Gln1714Ter
NM_001370404.1:c.5008C>T	NP_001357333.1:p.Gln1670Ter
NM_001370405.1:c.5011C>T	NP_001357334.1:p.Gln1671Ter
NM_001077183.3:c.4939C>T	NP_001070651.1:p.Gln1647Ter
NM_001114382.3:c.5071C>T	NP_001107854.1:p.Gln1691Ter
NM_001318827.2:c.4831C>T	NP_001305756.1:p.Gln1611Ter
NM_001318829.2:c.4795C>T	NP_001305758.1:p.Gln1599Ter
NM_001318831.2:c.4408C>T	NP_001305760.1:p.Gln1470Ter
NM_001318832.2:c.4972C>T	NP_001305761.1:p.Gln1658Ter
NM_001363528.2:c.4942C>T	NP_001350457.1:p.Gln1648Ter
NM_021055.3:c.5011C>T	NP_066399.2:p.Gln1671Ter