Canonical Allele Identifier: CA394304984

Gene: TSC2

Linked Data

• dbSNP Id: rs45517355
• gnomAD v4: 16-2085306-A-T
• MyVariant Identifiers: chr16:g.2135307A>T (hg19) ; chr16:g.2085306A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2085306A>T , CM000678.2:g.2085306A>T	GRCh38
NC_000016.9:g.2135307A>T , CM000678.1:g.2135307A>T	GRCh37
NC_000016.8:g.2075308A>T	NCBI36
NG_005895.1:g.41001A>T , LRG_487:g.41001A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*2995A>T	ENSP00000455997.2:n.*2995A>T
ENST00000642206.2:c.4493A>T	ENSP00000495146.2:p.Tyr1498Phe
ENST00000642365.2:c.4643A>T	ENSP00000495459.2:p.Tyr1548Phe
ENST00000644417.2:c.*5026A>T	ENSP00000493912.2:n.*5026A>T
ENST00000646464.2:c.*7395A>T	ENSP00000496610.2:n.*7395A>T
ENST00000219476.9:c.4646A>T MANE Select	ENSP00000219476.3:p.Tyr1549Phe
ENST00000350773.9:c.4577A>T	ENSP00000344383.4:p.Tyr1526Phe
ENST00000401874.7:c.4445A>T	ENSP00000384468.2:p.Tyr1482Phe
ENST00000568454.6:c.4478A>T	ENSP00000454487.1:p.Tyr1493Phe
ENST00000569110.2:c.869A>T
ENST00000569930.2:n.2528A>T
ENST00000642365.1:c.3300A>T
ENST00000642561.1:c.4517A>T	ENSP00000495099.1:p.Tyr1506Phe
ENST00000642728.1:n.828A>T
ENST00000642791.1:n.243A>T
ENST00000642797.1:c.4448A>T	ENSP00000493846.1:p.Tyr1483Phe
ENST00000642936.1:c.4514A>T	ENSP00000494514.1:p.Tyr1505Phe
ENST00000643088.1:c.4439A>T	ENSP00000494747.1:p.Tyr1480Phe
ENST00000643177.1:n.660A>T
ENST00000643426.1:n.2294A>T
ENST00000643946.1:c.4571A>T	ENSP00000495927.1:p.Tyr1524Phe
ENST00000644043.1:c.4517A>T	ENSP00000496262.1:p.Tyr1506Phe
ENST00000644278.1:n.128A>T
ENST00000644329.1:c.4445A>T	ENSP00000496611.1:p.Tyr1482Phe
ENST00000644335.1:c.4442A>T	ENSP00000496317.1:p.Tyr1481Phe
ENST00000644399.1:c.4567A>T
ENST00000645024.1:n.2730A>T
ENST00000646388.1:c.4640A>T	ENSP00000495921.1:p.Tyr1547Phe
ENST00000646634.1:n.3461A>T
ENST00000646674.1:n.1898A>T
ENST00000647042.1:n.1869A>T
ENST00000647180.1:n.1759A>T
ENST00000219476.7:c.4646A>T	ENSP00000219476.3:p.Tyr1549Phe
ENST00000350773.8:c.4577A>T	ENSP00000344383.4:p.Tyr1526Phe
ENST00000382538.10:c.4301A>T	ENSP00000371978.6:p.Tyr1434Phe
ENST00000401874.6:c.4445A>T	ENSP00000384468.2:p.Tyr1482Phe
ENST00000439117.6:c.*3813A>T	ENSP00000406980.2:n.*3813A>T
ENST00000439673.6:c.4337A>T	ENSP00000399232.2:p.Tyr1446Phe
ENST00000497886.5:n.2404A>T
ENST00000568454.5:c.4478A>T	ENSP00000454487.1:p.Tyr1493Phe
ENST00000569110.1:c.828A>T
ENST00000569930.1:n.1761A>T
NM_000548.3:c.4646A>T , LRG_487t1:c.4646A>T	NP_000539.2:p.Tyr1549Phe
NM_001077183.1:c.4445A>T	NP_001070651.1:p.Tyr1482Phe
NM_001114382.1:c.4577A>T	NP_001107854.1:p.Tyr1526Phe
XM_005255529.3:c.4517A>T	XP_005255586.2:p.Tyr1506Phe
XM_005255531.3:c.4448A>T	XP_005255588.2:p.Tyr1483Phe
XM_011522636.1:c.4700A>T	XP_011520938.1:p.Tyr1567Phe
XM_011522637.1:c.4697A>T	XP_011520939.1:p.Tyr1566Phe
XM_011522638.1:c.4589A>T	XP_011520940.1:p.Tyr1530Phe
XM_011522639.1:c.4571A>T	XP_011520941.1:p.Tyr1524Phe
XM_011522640.1:c.4568A>T	XP_011520942.1:p.Tyr1523Phe
XM_011522641.1:c.4337A>T	XP_011520943.1:p.Tyr1446Phe
NM_000548.4:c.4646A>T	NP_000539.2:p.Tyr1549Phe
NM_001077183.2:c.4445A>T	NP_001070651.1:p.Tyr1482Phe
NM_001114382.2:c.4577A>T	NP_001107854.1:p.Tyr1526Phe
NM_001318827.1:c.4337A>T	NP_001305756.1:p.Tyr1446Phe
NM_001318829.1:c.4301A>T	NP_001305758.1:p.Tyr1434Phe
NM_001318831.1:c.3914A>T	NP_001305760.1:p.Tyr1305Phe
NM_001318832.1:c.4478A>T	NP_001305761.1:p.Tyr1493Phe
NM_001363528.1:c.4448A>T	NP_001350457.1:p.Tyr1483Phe
NM_021055.2:c.4517A>T	NP_066399.2:p.Tyr1506Phe
XM_005255531.4:c.4448A>T	XP_005255588.2:p.Tyr1483Phe
XM_011522636.2:c.4700A>T	XP_011520938.1:p.Tyr1567Phe
XM_011522637.2:c.4697A>T	XP_011520939.1:p.Tyr1566Phe
XM_011522638.2:c.4862A>T	XP_011520940.2:p.Tyr1621Phe
XM_011522639.2:c.4571A>T	XP_011520941.1:p.Tyr1524Phe
XM_011522640.2:c.4568A>T	XP_011520942.1:p.Tyr1523Phe
XM_017023615.1:c.4643A>T	XP_016879104.1:p.Tyr1548Phe
XM_017023616.1:c.4514A>T	XP_016879105.1:p.Tyr1505Phe
XM_017023617.1:c.4610A>T	XP_016879106.1:p.Tyr1537Phe
XM_017023618.1:c.3356A>T	XP_016879107.1:p.Tyr1119Phe
XM_024450413.1:c.4445A>T	XP_024306181.1:p.Tyr1482Phe
NM_000548.5:c.4646A>T MANE Select	NP_000539.2:p.Tyr1549Phe
NM_001370404.1:c.4514A>T	NP_001357333.1:p.Tyr1505Phe
NM_001370405.1:c.4517A>T	NP_001357334.1:p.Tyr1506Phe
NM_001077183.3:c.4445A>T	NP_001070651.1:p.Tyr1482Phe
NM_001114382.3:c.4577A>T	NP_001107854.1:p.Tyr1526Phe
NM_001318827.2:c.4337A>T	NP_001305756.1:p.Tyr1446Phe
NM_001318829.2:c.4301A>T	NP_001305758.1:p.Tyr1434Phe
NM_001318831.2:c.3914A>T	NP_001305760.1:p.Tyr1305Phe
NM_001318832.2:c.4478A>T	NP_001305761.1:p.Tyr1493Phe
NM_001363528.2:c.4448A>T	NP_001350457.1:p.Tyr1483Phe
NM_021055.3:c.4517A>T	NP_066399.2:p.Tyr1506Phe