Canonical Allele Identifier: CA620705905

Gene: TSC2

Linked Data

• ClinVar Variation Id: 467901
• ClinVar RCV Id: RCV000554315 ; RCV003302846
• dbSNP Id: rs1246472342
• gnomAD v2: 16-2120583-T-C
• MyVariant Identifiers: chr16:g.2120583T>C (hg19) ; chr16:g.2070582T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2070582T>C , CM000678.2:g.2070582T>C	GRCh38
NC_000016.9:g.2120583T>C , CM000678.1:g.2120583T>C	GRCh37
NC_000016.8:g.2060584T>C	NCBI36
NG_005895.1:g.26277T>C , LRG_487:g.26277T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*386+4T>C	ENSP00000455997.2:n.*386+4T>C
ENST00000642206.2:c.1884+4T>C	ENSP00000495146.2:n.1884+4T>C
ENST00000642365.2:c.1839+4T>C	ENSP00000495459.2:n.1839+4T>C
ENST00000644417.2:c.*1276+4T>C	ENSP00000493912.2:n.*1276+4T>C
ENST00000646464.2:c.*1444+4T>C	ENSP00000496610.2:n.*1444+4T>C
ENST00000219476.9:c.1839+4T>C MANE Select	ENSP00000219476.3:n.1839+4T>C
ENST00000350773.9:c.1839+4T>C	ENSP00000344383.4:n.1839+4T>C
ENST00000401874.7:c.1839+4T>C	ENSP00000384468.2:n.1839+4T>C
ENST00000568454.6:c.1872+4T>C	ENSP00000454487.1:n.1872+4T>C
ENST00000642365.1:c.496+4T>C
ENST00000642561.1:c.1839+4T>C	ENSP00000495099.1:n.1839+4T>C
ENST00000642797.1:c.1839+4T>C	ENSP00000493846.1:n.1839+4T>C
ENST00000642936.1:c.1839+4T>C	ENSP00000494514.1:n.1839+4T>C
ENST00000643088.1:c.1839+4T>C	ENSP00000494747.1:n.1839+4T>C
ENST00000643298.1:c.*1341+4T>C	ENSP00000494393.1:n.*1341+4T>C
ENST00000643946.1:c.1839+4T>C	ENSP00000495927.1:n.1839+4T>C
ENST00000644043.1:c.1839+4T>C	ENSP00000496262.1:n.1839+4T>C
ENST00000644135.1:c.*339+4T>C	ENSP00000495644.1:n.*339+4T>C
ENST00000644329.1:c.1839+4T>C	ENSP00000496611.1:n.1839+4T>C
ENST00000644335.1:c.1839+4T>C	ENSP00000496317.1:n.1839+4T>C
ENST00000644399.1:c.1832+4T>C
ENST00000644847.1:n.831+4T>C
ENST00000645552.1:n.119+4T>C
ENST00000646388.1:c.1839+4T>C	ENSP00000495921.1:n.1839+4T>C
ENST00000646634.1:n.852+4T>C
ENST00000219476.7:c.1839+4T>C	ENSP00000219476.3:n.1839+4T>C
ENST00000350773.8:c.1839+4T>C	ENSP00000344383.4:n.1839+4T>C
ENST00000382538.10:c.1692+4T>C	ENSP00000371978.6:n.1692+4T>C
ENST00000401874.6:c.1839+4T>C	ENSP00000384468.2:n.1839+4T>C
ENST00000439117.6:c.*1138+4T>C	ENSP00000406980.2:n.*1138+4T>C
ENST00000439673.6:c.1728+4T>C	ENSP00000399232.2:n.1728+4T>C
ENST00000488675.5:n.346+4T>C
ENST00000562474.1:n.564+4T>C
ENST00000568454.5:c.1872+4T>C	ENSP00000454487.1:n.1872+4T>C
ENST00000568566.5:c.479+4T>C	ENSP00000455997.1:n.479+4T>C
NM_000548.3:c.1839+4T>C , LRG_487t1:c.1839+4T>C	NP_000539.2:n.1839+4T>C
NM_001077183.1:c.1839+4T>C	NP_001070651.1:n.1839+4T>C
NM_001114382.1:c.1839+4T>C	NP_001107854.1:n.1839+4T>C
XM_005255529.3:c.1839+4T>C	XP_005255586.2:n.1839+4T>C
XM_005255531.3:c.1839+4T>C	XP_005255588.2:n.1839+4T>C
XM_011522636.1:c.1839+4T>C	XP_011520938.1:n.1839+4T>C
XM_011522637.1:c.1839+4T>C	XP_011520939.1:n.1839+4T>C
XM_011522638.1:c.1728+4T>C	XP_011520940.1:n.1728+4T>C
XM_011522639.1:c.1839+4T>C	XP_011520941.1:n.1839+4T>C
XM_011522640.1:c.1839+4T>C	XP_011520942.1:n.1839+4T>C
XM_011522641.1:c.1728+4T>C	XP_011520943.1:n.1728+4T>C
NM_000548.4:c.1839+4T>C	NP_000539.2:n.1839+4T>C
NM_001077183.2:c.1839+4T>C	NP_001070651.1:n.1839+4T>C
NM_001114382.2:c.1839+4T>C	NP_001107854.1:n.1839+4T>C
NM_001318827.1:c.1728+4T>C	NP_001305756.1:n.1728+4T>C
NM_001318829.1:c.1692+4T>C	NP_001305758.1:n.1692+4T>C
NM_001318831.1:c.1239+4T>C	NP_001305760.1:n.1239+4T>C
NM_001318832.1:c.1872+4T>C	NP_001305761.1:n.1872+4T>C
NM_001363528.1:c.1839+4T>C	NP_001350457.1:n.1839+4T>C
NM_021055.2:c.1839+4T>C	NP_066399.2:n.1839+4T>C
XM_005255531.4:c.1839+4T>C	XP_005255588.2:n.1839+4T>C
XM_011522636.2:c.1839+4T>C	XP_011520938.1:n.1839+4T>C
XM_011522637.2:c.1839+4T>C	XP_011520939.1:n.1839+4T>C
XM_011522638.2:c.2001+4T>C	XP_011520940.2:n.2001+4T>C
XM_011522639.2:c.1839+4T>C	XP_011520941.1:n.1839+4T>C
XM_011522640.2:c.1839+4T>C	XP_011520942.1:n.1839+4T>C
XM_017023615.1:c.1839+4T>C	XP_016879104.1:n.1839+4T>C
XM_017023616.1:c.1839+4T>C	XP_016879105.1:n.1839+4T>C
XM_017023617.1:c.2001+4T>C	XP_016879106.1:n.2001+4T>C
XM_017023618.1:c.495+4T>C	XP_016879107.1:n.495+4T>C
XM_024450413.1:c.1839+4T>C	XP_024306181.1:n.1839+4T>C
NM_000548.5:c.1839+4T>C MANE Select	NP_000539.2:n.1839+4T>C
NM_001370404.1:c.1839+4T>C	NP_001357333.1:n.1839+4T>C
NM_001370405.1:c.1839+4T>C	NP_001357334.1:n.1839+4T>C
NM_001077183.3:c.1839+4T>C	NP_001070651.1:n.1839+4T>C
NM_001114382.3:c.1839+4T>C	NP_001107854.1:n.1839+4T>C
NM_001318827.2:c.1728+4T>C	NP_001305756.1:n.1728+4T>C
NM_001318829.2:c.1692+4T>C	NP_001305758.1:n.1692+4T>C
NM_001318831.2:c.1239+4T>C	NP_001305760.1:n.1239+4T>C
NM_001318832.2:c.1872+4T>C	NP_001305761.1:n.1872+4T>C
NM_001363528.2:c.1839+4T>C	NP_001350457.1:n.1839+4T>C
NM_021055.3:c.1839+4T>C	NP_066399.2:n.1839+4T>C