Canonical Allele Identifier: CA394308816

Gene: TSC2

Linked Data

• MyVariant Identifiers: chr16:g.2136831T>G (hg19) ; chr16:g.2086830T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2086830T>G , CM000678.2:g.2086830T>G	GRCh38
NC_000016.9:g.2136831T>G , CM000678.1:g.2136831T>G	GRCh37
NC_000016.8:g.2076832T>G	NCBI36
NG_005895.1:g.42525T>G , LRG_487:g.42525T>G
NG_008617.1:g.56391A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*3297T>G	ENSP00000455997.2:n.*3297T>G
ENST00000642206.2:c.4795T>G	ENSP00000495146.2:p.Tyr1599Asp
ENST00000642365.2:c.4945T>G	ENSP00000495459.2:p.Tyr1649Asp
ENST00000644417.2:c.*5461T>G	ENSP00000493912.2:n.*5461T>G
ENST00000646464.2:c.*7697T>G	ENSP00000496610.2:n.*7697T>G
ENST00000219476.9:c.4948T>G MANE Select	ENSP00000219476.3:p.Tyr1650Asp
ENST00000350773.9:c.4879T>G	ENSP00000344383.4:p.Tyr1627Asp
ENST00000401874.7:c.4747T>G	ENSP00000384468.2:p.Tyr1583Asp
ENST00000568454.6:c.4780T>G	ENSP00000454487.1:p.Tyr1594Asp
ENST00000569110.2:c.1171T>G
ENST00000569930.2:n.2830T>G
ENST00000642365.1:c.3602T>G
ENST00000642561.1:c.4819T>G	ENSP00000495099.1:p.Tyr1607Asp
ENST00000642728.1:n.1130T>G
ENST00000642791.1:n.545T>G
ENST00000642797.1:c.4750T>G	ENSP00000493846.1:p.Tyr1584Asp
ENST00000642936.1:c.4816T>G	ENSP00000494514.1:p.Tyr1606Asp
ENST00000643088.1:c.4741T>G	ENSP00000494747.1:p.Tyr1581Asp
ENST00000643177.1:n.962T>G
ENST00000643426.1:n.2596T>G
ENST00000643946.1:c.4873T>G	ENSP00000495927.1:p.Tyr1625Asp
ENST00000644043.1:c.4819T>G	ENSP00000496262.1:p.Tyr1607Asp
ENST00000644278.1:n.430T>G
ENST00000644329.1:c.4747T>G	ENSP00000496611.1:p.Tyr1583Asp
ENST00000644335.1:c.4744T>G	ENSP00000496317.1:p.Tyr1582Asp
ENST00000644399.1:c.4869T>G
ENST00000645024.1:n.3032T>G
ENST00000646388.1:c.4942T>G	ENSP00000495921.1:p.Tyr1648Asp
ENST00000646557.1:n.109T>G
ENST00000646634.1:n.3763T>G
ENST00000646674.1:n.2200T>G
ENST00000647042.1:n.2171T>G
ENST00000647180.1:n.2061T>G
ENST00000219476.7:c.4948T>G	ENSP00000219476.3:p.Tyr1650Asp
ENST00000350773.8:c.4879T>G	ENSP00000344383.4:p.Tyr1627Asp
ENST00000382538.10:c.4603T>G	ENSP00000371978.6:p.Tyr1535Asp
ENST00000401874.6:c.4747T>G	ENSP00000384468.2:p.Tyr1583Asp
ENST00000439117.6:c.*4115T>G	ENSP00000406980.2:n.*4115T>G
ENST00000439673.6:c.4639T>G	ENSP00000399232.2:p.Tyr1547Asp
ENST00000497886.5:n.2671T>G
ENST00000568454.5:c.4780T>G	ENSP00000454487.1:p.Tyr1594Asp
ENST00000569110.1:c.1130T>G
ENST00000569930.1:n.2063T>G
NM_000548.3:c.4948T>G , LRG_487t1:c.4948T>G	NP_000539.2:p.Tyr1650Asp
NM_001077183.1:c.4747T>G	NP_001070651.1:p.Tyr1583Asp
NM_001114382.1:c.4879T>G	NP_001107854.1:p.Tyr1627Asp
XM_005255529.3:c.4819T>G	XP_005255586.2:p.Tyr1607Asp
XM_005255531.3:c.4750T>G	XP_005255588.2:p.Tyr1584Asp
XM_011522636.1:c.5002T>G	XP_011520938.1:p.Tyr1668Asp
XM_011522637.1:c.4999T>G	XP_011520939.1:p.Tyr1667Asp
XM_011522638.1:c.4891T>G	XP_011520940.1:p.Tyr1631Asp
XM_011522639.1:c.4873T>G	XP_011520941.1:p.Tyr1625Asp
XM_011522640.1:c.4870T>G	XP_011520942.1:p.Tyr1624Asp
XM_011522641.1:c.4639T>G	XP_011520943.1:p.Tyr1547Asp
NM_000548.4:c.4948T>G	NP_000539.2:p.Tyr1650Asp
NM_001077183.2:c.4747T>G	NP_001070651.1:p.Tyr1583Asp
NM_001114382.2:c.4879T>G	NP_001107854.1:p.Tyr1627Asp
NM_001318827.1:c.4639T>G	NP_001305756.1:p.Tyr1547Asp
NM_001318829.1:c.4603T>G	NP_001305758.1:p.Tyr1535Asp
NM_001318831.1:c.4216T>G	NP_001305760.1:p.Tyr1406Asp
NM_001318832.1:c.4780T>G	NP_001305761.1:p.Tyr1594Asp
NM_001363528.1:c.4750T>G	NP_001350457.1:p.Tyr1584Asp
NM_021055.2:c.4819T>G	NP_066399.2:p.Tyr1607Asp
XM_005255531.4:c.4750T>G	XP_005255588.2:p.Tyr1584Asp
XM_011522636.2:c.5002T>G	XP_011520938.1:p.Tyr1668Asp
XM_011522637.2:c.4999T>G	XP_011520939.1:p.Tyr1667Asp
XM_011522638.2:c.5164T>G	XP_011520940.2:p.Tyr1722Asp
XM_011522639.2:c.4873T>G	XP_011520941.1:p.Tyr1625Asp
XM_011522640.2:c.4870T>G	XP_011520942.1:p.Tyr1624Asp
XM_017023615.1:c.4945T>G	XP_016879104.1:p.Tyr1649Asp
XM_017023616.1:c.4816T>G	XP_016879105.1:p.Tyr1606Asp
XM_017023617.1:c.4912T>G	XP_016879106.1:p.Tyr1638Asp
XM_017023618.1:c.3658T>G	XP_016879107.1:p.Tyr1220Asp
XM_024450413.1:c.4747T>G	XP_024306181.1:p.Tyr1583Asp
NM_000548.5:c.4948T>G MANE Select	NP_000539.2:p.Tyr1650Asp
NM_001370404.1:c.4816T>G	NP_001357333.1:p.Tyr1606Asp
NM_001370405.1:c.4819T>G	NP_001357334.1:p.Tyr1607Asp
NM_001077183.3:c.4747T>G	NP_001070651.1:p.Tyr1583Asp
NM_001114382.3:c.4879T>G	NP_001107854.1:p.Tyr1627Asp
NM_001318827.2:c.4639T>G	NP_001305756.1:p.Tyr1547Asp
NM_001318829.2:c.4603T>G	NP_001305758.1:p.Tyr1535Asp
NM_001318831.2:c.4216T>G	NP_001305760.1:p.Tyr1406Asp
NM_001318832.2:c.4780T>G	NP_001305761.1:p.Tyr1594Asp
NM_001363528.2:c.4750T>G	NP_001350457.1:p.Tyr1584Asp
NM_021055.3:c.4819T>G	NP_066399.2:p.Tyr1607Asp