Canonical Allele Identifier: CA052718

Gene: TSC2

Linked Data

• ClinVar Variation Id: 1429204
• ClinVar RCV Id: RCV001950035
• dbSNP Id: rs762819541
• ExAC: 16:2136379 A / G
• gnomAD v2: 16-2136379-A-G
• gnomAD v4: 16-2086378-A-G
• MyVariant Identifiers: chr16:g.2136379A>G (hg19) ; chr16:g.2086378A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2086378A>G , CM000678.2:g.2086378A>G	GRCh38
NC_000016.9:g.2136379A>G , CM000678.1:g.2136379A>G	GRCh37
NC_000016.8:g.2076380A>G	NCBI36
NG_005895.1:g.42073A>G , LRG_487:g.42073A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000568566.6:c.*3197A>G	ENSP00000455997.2:n.*3197A>G
ENST00000642206.2:c.4695A>G	ENSP00000495146.2:p.Gln1565=
ENST00000642365.2:c.4845A>G	ENSP00000495459.2:p.Gln1615=
ENST00000644417.2:c.*5361A>G	ENSP00000493912.2:n.*5361A>G
ENST00000646464.2:c.*7597A>G	ENSP00000496610.2:n.*7597A>G
ENST00000219476.9:c.4848A>G MANE Select	ENSP00000219476.3:p.Gln1616=
ENST00000350773.9:c.4779A>G	ENSP00000344383.4:p.Gln1593=
ENST00000401874.7:c.4647A>G	ENSP00000384468.2:p.Gln1549=
ENST00000568454.6:c.4680A>G	ENSP00000454487.1:p.Gln1560=
ENST00000569110.2:c.1071A>G
ENST00000569930.2:n.2730A>G
ENST00000642365.1:c.3502A>G
ENST00000642561.1:c.4719A>G	ENSP00000495099.1:p.Gln1573=
ENST00000642728.1:n.1030A>G
ENST00000642791.1:n.445A>G
ENST00000642797.1:c.4650A>G	ENSP00000493846.1:p.Gln1550=
ENST00000642936.1:c.4716A>G	ENSP00000494514.1:p.Gln1572=
ENST00000643088.1:c.4641A>G	ENSP00000494747.1:p.Gln1547=
ENST00000643177.1:n.862A>G
ENST00000643426.1:n.2496A>G
ENST00000643946.1:c.4773A>G	ENSP00000495927.1:p.Gln1591=
ENST00000644043.1:c.4719A>G	ENSP00000496262.1:p.Gln1573=
ENST00000644278.1:n.330A>G
ENST00000644329.1:c.4647A>G	ENSP00000496611.1:p.Gln1549=
ENST00000644335.1:c.4644A>G	ENSP00000496317.1:p.Gln1548=
ENST00000644399.1:c.4769A>G
ENST00000645024.1:n.2932A>G
ENST00000646388.1:c.4842A>G	ENSP00000495921.1:p.Gln1614=
ENST00000646557.1:n.9A>G
ENST00000646634.1:n.3663A>G
ENST00000646674.1:n.2100A>G
ENST00000647042.1:n.2071A>G
ENST00000647180.1:n.1961A>G
ENST00000219476.7:c.4848A>G	ENSP00000219476.3:p.Gln1616=
ENST00000350773.8:c.4779A>G	ENSP00000344383.4:p.Gln1593=
ENST00000382538.10:c.4503A>G	ENSP00000371978.6:p.Gln1501=
ENST00000401874.6:c.4647A>G	ENSP00000384468.2:p.Gln1549=
ENST00000439117.6:c.*4015A>G	ENSP00000406980.2:n.*4015A>G
ENST00000439673.6:c.4539A>G	ENSP00000399232.2:p.Gln1513=
ENST00000497886.5:n.2606A>G
ENST00000568454.5:c.4680A>G	ENSP00000454487.1:p.Gln1560=
ENST00000569110.1:c.1030A>G
ENST00000569930.1:n.1963A>G
NM_000548.3:c.4848A>G , LRG_487t1:c.4848A>G	NP_000539.2:p.Gln1616=
NM_001077183.1:c.4647A>G	NP_001070651.1:p.Gln1549=
NM_001114382.1:c.4779A>G	NP_001107854.1:p.Gln1593=
XM_005255529.3:c.4719A>G	XP_005255586.2:p.Gln1573=
XM_005255531.3:c.4650A>G	XP_005255588.2:p.Gln1550=
XM_011522636.1:c.4902A>G	XP_011520938.1:p.Gln1634=
XM_011522637.1:c.4899A>G	XP_011520939.1:p.Gln1633=
XM_011522638.1:c.4791A>G	XP_011520940.1:p.Gln1597=
XM_011522639.1:c.4773A>G	XP_011520941.1:p.Gln1591=
XM_011522640.1:c.4770A>G	XP_011520942.1:p.Gln1590=
XM_011522641.1:c.4539A>G	XP_011520943.1:p.Gln1513=
NM_000548.4:c.4848A>G	NP_000539.2:p.Gln1616=
NM_001077183.2:c.4647A>G	NP_001070651.1:p.Gln1549=
NM_001114382.2:c.4779A>G	NP_001107854.1:p.Gln1593=
NM_001318827.1:c.4539A>G	NP_001305756.1:p.Gln1513=
NM_001318829.1:c.4503A>G	NP_001305758.1:p.Gln1501=
NM_001318831.1:c.4116A>G	NP_001305760.1:p.Gln1372=
NM_001318832.1:c.4680A>G	NP_001305761.1:p.Gln1560=
NM_001363528.1:c.4650A>G	NP_001350457.1:p.Gln1550=
NM_021055.2:c.4719A>G	NP_066399.2:p.Gln1573=
XM_005255531.4:c.4650A>G	XP_005255588.2:p.Gln1550=
XM_011522636.2:c.4902A>G	XP_011520938.1:p.Gln1634=
XM_011522637.2:c.4899A>G	XP_011520939.1:p.Gln1633=
XM_011522638.2:c.5064A>G	XP_011520940.2:p.Gln1688=
XM_011522639.2:c.4773A>G	XP_011520941.1:p.Gln1591=
XM_011522640.2:c.4770A>G	XP_011520942.1:p.Gln1590=
XM_017023615.1:c.4845A>G	XP_016879104.1:p.Gln1615=
XM_017023616.1:c.4716A>G	XP_016879105.1:p.Gln1572=
XM_017023617.1:c.4812A>G	XP_016879106.1:p.Gln1604=
XM_017023618.1:c.3558A>G	XP_016879107.1:p.Gln1186=
XM_024450413.1:c.4647A>G	XP_024306181.1:p.Gln1549=
NM_000548.5:c.4848A>G MANE Select	NP_000539.2:p.Gln1616=
NM_001370404.1:c.4716A>G	NP_001357333.1:p.Gln1572=
NM_001370405.1:c.4719A>G	NP_001357334.1:p.Gln1573=
NM_001077183.3:c.4647A>G	NP_001070651.1:p.Gln1549=
NM_001114382.3:c.4779A>G	NP_001107854.1:p.Gln1593=
NM_001318827.2:c.4539A>G	NP_001305756.1:p.Gln1513=
NM_001318829.2:c.4503A>G	NP_001305758.1:p.Gln1501=
NM_001318831.2:c.4116A>G	NP_001305760.1:p.Gln1372=
NM_001318832.2:c.4680A>G	NP_001305761.1:p.Gln1560=
NM_001363528.2:c.4650A>G	NP_001350457.1:p.Gln1550=
NM_021055.3:c.4719A>G	NP_066399.2:p.Gln1573=