Canonical Allele Identifier: CA052706

Gene: TSC2

Linked Data

• dbSNP Id: rs752798361
• ExAC: 16:2136374 A / T
• gnomAD v2: 16-2136374-A-T
• MyVariant Identifiers: chr16:g.2136374A>T (hg19) ; chr16:g.2086373A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2086373A>T , CM000678.2:g.2086373A>T	GRCh38
NC_000016.9:g.2136374A>T , CM000678.1:g.2136374A>T	GRCh37
NC_000016.8:g.2076375A>T	NCBI36
NG_005895.1:g.42068A>T , LRG_487:g.42068A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000568566.6:c.*3192A>T	ENSP00000455997.2:n.*3192A>T
ENST00000642206.2:c.4690A>T	ENSP00000495146.2:p.Met1564Leu
ENST00000642365.2:c.4840A>T	ENSP00000495459.2:p.Met1614Leu
ENST00000644417.2:c.*5356A>T	ENSP00000493912.2:n.*5356A>T
ENST00000646464.2:c.*7592A>T	ENSP00000496610.2:n.*7592A>T
ENST00000219476.9:c.4843A>T MANE Select	ENSP00000219476.3:p.Met1615Leu
ENST00000350773.9:c.4774A>T	ENSP00000344383.4:p.Met1592Leu
ENST00000401874.7:c.4642A>T	ENSP00000384468.2:p.Met1548Leu
ENST00000568454.6:c.4675A>T	ENSP00000454487.1:p.Met1559Leu
ENST00000569110.2:c.1066A>T
ENST00000569930.2:n.2725A>T
ENST00000642365.1:c.3497A>T
ENST00000642561.1:c.4714A>T	ENSP00000495099.1:p.Met1572Leu
ENST00000642728.1:n.1025A>T
ENST00000642791.1:n.440A>T
ENST00000642797.1:c.4645A>T	ENSP00000493846.1:p.Met1549Leu
ENST00000642936.1:c.4711A>T	ENSP00000494514.1:p.Met1571Leu
ENST00000643088.1:c.4636A>T	ENSP00000494747.1:p.Met1546Leu
ENST00000643177.1:n.857A>T
ENST00000643426.1:n.2491A>T
ENST00000643946.1:c.4768A>T	ENSP00000495927.1:p.Met1590Leu
ENST00000644043.1:c.4714A>T	ENSP00000496262.1:p.Met1572Leu
ENST00000644278.1:n.325A>T
ENST00000644329.1:c.4642A>T	ENSP00000496611.1:p.Met1548Leu
ENST00000644335.1:c.4639A>T	ENSP00000496317.1:p.Met1547Leu
ENST00000644399.1:c.4764A>T
ENST00000645024.1:n.2927A>T
ENST00000646388.1:c.4837A>T	ENSP00000495921.1:p.Met1613Leu
ENST00000646557.1:n.4A>T
ENST00000646634.1:n.3658A>T
ENST00000646674.1:n.2095A>T
ENST00000647042.1:n.2066A>T
ENST00000647180.1:n.1956A>T
ENST00000219476.7:c.4843A>T	ENSP00000219476.3:p.Met1615Leu
ENST00000350773.8:c.4774A>T	ENSP00000344383.4:p.Met1592Leu
ENST00000382538.10:c.4498A>T	ENSP00000371978.6:p.Met1500Leu
ENST00000401874.6:c.4642A>T	ENSP00000384468.2:p.Met1548Leu
ENST00000439117.6:c.*4010A>T	ENSP00000406980.2:n.*4010A>T
ENST00000439673.6:c.4534A>T	ENSP00000399232.2:p.Met1512Leu
ENST00000497886.5:n.2601A>T
ENST00000568454.5:c.4675A>T	ENSP00000454487.1:p.Met1559Leu
ENST00000569110.1:c.1025A>T
ENST00000569930.1:n.1958A>T
NM_000548.3:c.4843A>T , LRG_487t1:c.4843A>T	NP_000539.2:p.Met1615Leu
NM_001077183.1:c.4642A>T	NP_001070651.1:p.Met1548Leu
NM_001114382.1:c.4774A>T	NP_001107854.1:p.Met1592Leu
XM_005255529.3:c.4714A>T	XP_005255586.2:p.Met1572Leu
XM_005255531.3:c.4645A>T	XP_005255588.2:p.Met1549Leu
XM_011522636.1:c.4897A>T	XP_011520938.1:p.Met1633Leu
XM_011522637.1:c.4894A>T	XP_011520939.1:p.Met1632Leu
XM_011522638.1:c.4786A>T	XP_011520940.1:p.Met1596Leu
XM_011522639.1:c.4768A>T	XP_011520941.1:p.Met1590Leu
XM_011522640.1:c.4765A>T	XP_011520942.1:p.Met1589Leu
XM_011522641.1:c.4534A>T	XP_011520943.1:p.Met1512Leu
NM_000548.4:c.4843A>T	NP_000539.2:p.Met1615Leu
NM_001077183.2:c.4642A>T	NP_001070651.1:p.Met1548Leu
NM_001114382.2:c.4774A>T	NP_001107854.1:p.Met1592Leu
NM_001318827.1:c.4534A>T	NP_001305756.1:p.Met1512Leu
NM_001318829.1:c.4498A>T	NP_001305758.1:p.Met1500Leu
NM_001318831.1:c.4111A>T	NP_001305760.1:p.Met1371Leu
NM_001318832.1:c.4675A>T	NP_001305761.1:p.Met1559Leu
NM_001363528.1:c.4645A>T	NP_001350457.1:p.Met1549Leu
NM_021055.2:c.4714A>T	NP_066399.2:p.Met1572Leu
XM_005255531.4:c.4645A>T	XP_005255588.2:p.Met1549Leu
XM_011522636.2:c.4897A>T	XP_011520938.1:p.Met1633Leu
XM_011522637.2:c.4894A>T	XP_011520939.1:p.Met1632Leu
XM_011522638.2:c.5059A>T	XP_011520940.2:p.Met1687Leu
XM_011522639.2:c.4768A>T	XP_011520941.1:p.Met1590Leu
XM_011522640.2:c.4765A>T	XP_011520942.1:p.Met1589Leu
XM_017023615.1:c.4840A>T	XP_016879104.1:p.Met1614Leu
XM_017023616.1:c.4711A>T	XP_016879105.1:p.Met1571Leu
XM_017023617.1:c.4807A>T	XP_016879106.1:p.Met1603Leu
XM_017023618.1:c.3553A>T	XP_016879107.1:p.Met1185Leu
XM_024450413.1:c.4642A>T	XP_024306181.1:p.Met1548Leu
NM_000548.5:c.4843A>T MANE Select	NP_000539.2:p.Met1615Leu
NM_001370404.1:c.4711A>T	NP_001357333.1:p.Met1571Leu
NM_001370405.1:c.4714A>T	NP_001357334.1:p.Met1572Leu
NM_001077183.3:c.4642A>T	NP_001070651.1:p.Met1548Leu
NM_001114382.3:c.4774A>T	NP_001107854.1:p.Met1592Leu
NM_001318827.2:c.4534A>T	NP_001305756.1:p.Met1512Leu
NM_001318829.2:c.4498A>T	NP_001305758.1:p.Met1500Leu
NM_001318831.2:c.4111A>T	NP_001305760.1:p.Met1371Leu
NM_001318832.2:c.4675A>T	NP_001305761.1:p.Met1559Leu
NM_001363528.2:c.4645A>T	NP_001350457.1:p.Met1549Leu
NM_021055.3:c.4714A>T	NP_066399.2:p.Met1572Leu