Canonical Allele Identifier: CA022636

Gene: TSC2

Linked Data

• ClinVar Variation Id: 64873
• ClinVar RCV Id: RCV000055073 ; RCV000557913 ; RCV001529485 ; RCV003466926 ; RCV002354246
• dbSNP Id: rs397514899
• gnomAD v4: 16-2055522-A-G
• MyVariant Identifiers: chr16:g.2105523A>G (hg19) ; chr16:g.2055522A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2055522A>G , CM000678.2:g.2055522A>G	GRCh38
NC_000016.9:g.2105523A>G , CM000678.1:g.2105523A>G	GRCh37
NC_000016.8:g.2045524A>G	NCBI36
NG_005895.1:g.11217A>G , LRG_487:g.11217A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.599+3A>G	ENSP00000455997.2:n.599+3A>G
ENST00000642206.2:c.644+3A>G	ENSP00000495146.2:n.644+3A>G
ENST00000642365.2:c.599+3A>G	ENSP00000495459.2:n.599+3A>G
ENST00000644417.2:c.*36+3A>G	ENSP00000493912.2:n.*36+3A>G
ENST00000646464.2:c.226-458A>G	ENSP00000496610.2:n.226-458A>G
ENST00000219476.9:c.599+3A>G MANE Select	ENSP00000219476.3:n.599+3A>G
ENST00000350773.9:c.599+3A>G	ENSP00000344383.4:n.599+3A>G
ENST00000401874.7:c.599+3A>G	ENSP00000384468.2:n.599+3A>G
ENST00000432909.3:c.373+3A>G
ENST00000461648.3:n.2516A>G
ENST00000568454.6:c.632+3A>G	ENSP00000454487.1:n.632+3A>G
ENST00000568692.2:n.1325A>G
ENST00000642561.1:c.599+3A>G	ENSP00000495099.1:n.599+3A>G
ENST00000642797.1:c.599+3A>G	ENSP00000493846.1:n.599+3A>G
ENST00000642812.1:n.656+3A>G
ENST00000642936.1:c.599+3A>G	ENSP00000494514.1:n.599+3A>G
ENST00000643088.1:c.599+3A>G	ENSP00000494747.1:n.599+3A>G
ENST00000643120.1:n.626A>G
ENST00000643149.1:n.1552+3A>G
ENST00000643298.1:c.599+3A>G	ENSP00000494393.1:n.599+3A>G
ENST00000643745.1:c.599+3A>G	ENSP00000495948.1:n.599+3A>G
ENST00000643946.1:c.599+3A>G	ENSP00000495927.1:n.599+3A>G
ENST00000644043.1:c.599+3A>G	ENSP00000496262.1:n.599+3A>G
ENST00000644135.1:c.599+3A>G	ENSP00000495644.1:n.599+3A>G
ENST00000644222.1:n.686+3A>G
ENST00000644329.1:c.599+3A>G	ENSP00000496611.1:n.599+3A>G
ENST00000644335.1:c.599+3A>G	ENSP00000496317.1:n.599+3A>G
ENST00000644399.1:c.592+3A>G
ENST00000644417.1:c.297+3A>G	ENSP00000493912.1:n.297+3A>G
ENST00000644665.1:n.716+3A>G
ENST00000645591.1:n.1570+3A>G
ENST00000646388.1:c.599+3A>G	ENSP00000495921.1:n.599+3A>G
ENST00000646823.1:n.987+3A>G
ENST00000647234.1:n.1300+3A>G
ENST00000647242.1:n.1267+3A>G
ENST00000219476.7:c.599+3A>G	ENSP00000219476.3:n.599+3A>G
ENST00000350773.8:c.599+3A>G	ENSP00000344383.4:n.599+3A>G
ENST00000382538.10:c.452+3A>G	ENSP00000371978.6:n.452+3A>G
ENST00000401874.6:c.599+3A>G	ENSP00000384468.2:n.599+3A>G
ENST00000439117.6:c.226-674A>G	ENSP00000406980.2:n.226-674A>G
ENST00000439673.6:c.488+3A>G	ENSP00000399232.2:n.488+3A>G
ENST00000568454.5:c.632+3A>G	ENSP00000454487.1:n.632+3A>G
ENST00000568692.1:n.266A>G
NM_000548.3:c.599+3A>G , LRG_487t1:c.599+3A>G	NP_000539.2:n.599+3A>G
NM_001077183.1:c.599+3A>G	NP_001070651.1:n.599+3A>G
NM_001114382.1:c.599+3A>G	NP_001107854.1:n.599+3A>G
XM_005255529.3:c.599+3A>G	XP_005255586.2:n.599+3A>G
XM_005255531.3:c.599+3A>G	XP_005255588.2:n.599+3A>G
XM_011522636.1:c.599+3A>G	XP_011520938.1:n.599+3A>G
XM_011522637.1:c.599+3A>G	XP_011520939.1:n.599+3A>G
XM_011522638.1:c.488+3A>G	XP_011520940.1:n.488+3A>G
XM_011522639.1:c.599+3A>G	XP_011520941.1:n.599+3A>G
XM_011522640.1:c.599+3A>G	XP_011520942.1:n.599+3A>G
XM_011522641.1:c.488+3A>G	XP_011520943.1:n.488+3A>G
NM_000548.4:c.599+3A>G	NP_000539.2:n.599+3A>G
NM_001077183.2:c.599+3A>G	NP_001070651.1:n.599+3A>G
NM_001114382.2:c.599+3A>G	NP_001107854.1:n.599+3A>G
NM_001318827.1:c.488+3A>G	NP_001305756.1:n.488+3A>G
NM_001318829.1:c.452+3A>G	NP_001305758.1:n.452+3A>G
NM_001318831.1:c.-1-674A>G	NP_001305760.1:n.-1-674A>G
NM_001318832.1:c.632+3A>G	NP_001305761.1:n.632+3A>G
NM_001363528.1:c.599+3A>G	NP_001350457.1:n.599+3A>G
NM_021055.2:c.599+3A>G	NP_066399.2:n.599+3A>G
XM_005255531.4:c.599+3A>G	XP_005255588.2:n.599+3A>G
XM_011522636.2:c.599+3A>G	XP_011520938.1:n.599+3A>G
XM_011522637.2:c.599+3A>G	XP_011520939.1:n.599+3A>G
XM_011522638.2:c.761+3A>G	XP_011520940.2:n.761+3A>G
XM_011522639.2:c.599+3A>G	XP_011520941.1:n.599+3A>G
XM_011522640.2:c.599+3A>G	XP_011520942.1:n.599+3A>G
XM_017023615.1:c.599+3A>G	XP_016879104.1:n.599+3A>G
XM_017023616.1:c.599+3A>G	XP_016879105.1:n.599+3A>G
XM_017023617.1:c.761+3A>G	XP_016879106.1:n.761+3A>G
XM_017023618.1:c.-833+3A>G	XP_016879107.1:n.-833+3A>G
XM_024450413.1:c.599+3A>G	XP_024306181.1:n.599+3A>G
NM_000548.5:c.599+3A>G MANE Select	NP_000539.2:n.599+3A>G
NM_001370404.1:c.599+3A>G	NP_001357333.1:n.599+3A>G
NM_001370405.1:c.599+3A>G	NP_001357334.1:n.599+3A>G
NM_001077183.3:c.599+3A>G	NP_001070651.1:n.599+3A>G
NM_001114382.3:c.599+3A>G	NP_001107854.1:n.599+3A>G
NM_001318827.2:c.488+3A>G	NP_001305756.1:n.488+3A>G
NM_001318829.2:c.452+3A>G	NP_001305758.1:n.452+3A>G
NM_001318831.2:c.-1-674A>G	NP_001305760.1:n.-1-674A>G
NM_001318832.2:c.632+3A>G	NP_001305761.1:n.632+3A>G
NM_001363528.2:c.599+3A>G	NP_001350457.1:n.599+3A>G
NM_021055.3:c.599+3A>G	NP_066399.2:n.599+3A>G