Canonical Allele Identifier: CA16614777

Gene: TSC2

Linked Data

• ClinVar Variation Id: 406119
• ClinVar RCV Id: RCV000463381
• dbSNP Id: rs1060500972
• MyVariant Identifiers: chr16:g.2135028G>T (hg19) ; chr16:g.2085027G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2085027G>T , CM000678.2:g.2085027G>T	GRCh38
NC_000016.9:g.2135028G>T , CM000678.1:g.2135028G>T	GRCh37
NC_000016.8:g.2075029G>T	NCBI36
NG_005895.1:g.40722G>T , LRG_487:g.40722G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*2918+1G>T	ENSP00000455997.2:n.*2918+1G>T
ENST00000642206.2:c.4416+1G>T	ENSP00000495146.2:n.4416+1G>T
ENST00000642365.2:c.4566+1G>T	ENSP00000495459.2:n.4566+1G>T
ENST00000644417.2:c.*4949+1G>T	ENSP00000493912.2:n.*4949+1G>T
ENST00000646464.2:c.*7318+1G>T	ENSP00000496610.2:n.*7318+1G>T
ENST00000219476.9:c.4569+1G>T MANE Select	ENSP00000219476.3:n.4569+1G>T
ENST00000350773.9:c.4500+1G>T	ENSP00000344383.4:n.4500+1G>T
ENST00000401874.7:c.4368+1G>T	ENSP00000384468.2:n.4368+1G>T
ENST00000568454.6:c.4401+1G>T	ENSP00000454487.1:n.4401+1G>T
ENST00000569110.2:c.792+1G>T
ENST00000569930.2:n.2451+1G>T
ENST00000642365.1:c.3223+1G>T
ENST00000642561.1:c.4440+1G>T	ENSP00000495099.1:n.4440+1G>T
ENST00000642728.1:n.751+1G>T
ENST00000642797.1:c.4371+1G>T	ENSP00000493846.1:n.4371+1G>T
ENST00000642936.1:c.4437+1G>T	ENSP00000494514.1:n.4437+1G>T
ENST00000643088.1:c.4368+1G>T	ENSP00000494747.1:n.4368+1G>T
ENST00000643177.1:n.583+1G>T
ENST00000643426.1:n.2217+1G>T
ENST00000643946.1:c.4500+1G>T	ENSP00000495927.1:n.4500+1G>T
ENST00000644043.1:c.4440+1G>T	ENSP00000496262.1:n.4440+1G>T
ENST00000644329.1:c.4368+1G>T	ENSP00000496611.1:n.4368+1G>T
ENST00000644335.1:c.4371+1G>T	ENSP00000496317.1:n.4371+1G>T
ENST00000644399.1:c.4490+1G>T
ENST00000645024.1:n.2653+1G>T
ENST00000646388.1:c.4569+1G>T	ENSP00000495921.1:n.4569+1G>T
ENST00000646634.1:n.3384+1G>T
ENST00000646674.1:n.1821+1G>T
ENST00000647042.1:n.1792+1G>T
ENST00000647180.1:n.1682+1G>T
ENST00000219476.7:c.4569+1G>T	ENSP00000219476.3:n.4569+1G>T
ENST00000350773.8:c.4500+1G>T	ENSP00000344383.4:n.4500+1G>T
ENST00000382538.10:c.4224+1G>T	ENSP00000371978.6:n.4224+1G>T
ENST00000401874.6:c.4368+1G>T	ENSP00000384468.2:n.4368+1G>T
ENST00000439117.6:c.*3736+1G>T	ENSP00000406980.2:n.*3736+1G>T
ENST00000439673.6:c.4260+1G>T	ENSP00000399232.2:n.4260+1G>T
ENST00000497886.5:n.2327+1G>T
ENST00000568454.5:c.4401+1G>T	ENSP00000454487.1:n.4401+1G>T
ENST00000569110.1:c.751+1G>T
ENST00000569930.1:n.1684+1G>T
NM_000548.3:c.4569+1G>T , LRG_487t1:c.4569+1G>T	NP_000539.2:n.4569+1G>T
NM_001077183.1:c.4368+1G>T	NP_001070651.1:n.4368+1G>T
NM_001114382.1:c.4500+1G>T	NP_001107854.1:n.4500+1G>T
XM_005255529.3:c.4440+1G>T	XP_005255586.2:n.4440+1G>T
XM_005255531.3:c.4371+1G>T	XP_005255588.2:n.4371+1G>T
XM_011522636.1:c.4623+1G>T	XP_011520938.1:n.4623+1G>T
XM_011522637.1:c.4620+1G>T	XP_011520939.1:n.4620+1G>T
XM_011522638.1:c.4512+1G>T	XP_011520940.1:n.4512+1G>T
XM_011522639.1:c.4494+1G>T	XP_011520941.1:n.4494+1G>T
XM_011522640.1:c.4491+1G>T	XP_011520942.1:n.4491+1G>T
XM_011522641.1:c.4260+1G>T	XP_011520943.1:n.4260+1G>T
NM_000548.4:c.4569+1G>T	NP_000539.2:n.4569+1G>T
NM_001077183.2:c.4368+1G>T	NP_001070651.1:n.4368+1G>T
NM_001114382.2:c.4500+1G>T	NP_001107854.1:n.4500+1G>T
NM_001318827.1:c.4260+1G>T	NP_001305756.1:n.4260+1G>T
NM_001318829.1:c.4224+1G>T	NP_001305758.1:n.4224+1G>T
NM_001318831.1:c.3837+1G>T	NP_001305760.1:n.3837+1G>T
NM_001318832.1:c.4401+1G>T	NP_001305761.1:n.4401+1G>T
NM_001363528.1:c.4371+1G>T	NP_001350457.1:n.4371+1G>T
NM_021055.2:c.4440+1G>T	NP_066399.2:n.4440+1G>T
XM_005255531.4:c.4371+1G>T	XP_005255588.2:n.4371+1G>T
XM_011522636.2:c.4623+1G>T	XP_011520938.1:n.4623+1G>T
XM_011522637.2:c.4620+1G>T	XP_011520939.1:n.4620+1G>T
XM_011522638.2:c.4785+1G>T	XP_011520940.2:n.4785+1G>T
XM_011522639.2:c.4494+1G>T	XP_011520941.1:n.4494+1G>T
XM_011522640.2:c.4491+1G>T	XP_011520942.1:n.4491+1G>T
XM_017023615.1:c.4566+1G>T	XP_016879104.1:n.4566+1G>T
XM_017023616.1:c.4437+1G>T	XP_016879105.1:n.4437+1G>T
XM_017023617.1:c.4533+1G>T	XP_016879106.1:n.4533+1G>T
XM_017023618.1:c.3279+1G>T	XP_016879107.1:n.3279+1G>T
XM_024450413.1:c.4368+1G>T	XP_024306181.1:n.4368+1G>T
NM_000548.5:c.4569+1G>T MANE Select	NP_000539.2:n.4569+1G>T
NM_001370404.1:c.4437+1G>T	NP_001357333.1:n.4437+1G>T
NM_001370405.1:c.4440+1G>T	NP_001357334.1:n.4440+1G>T
NM_001077183.3:c.4368+1G>T	NP_001070651.1:n.4368+1G>T
NM_001114382.3:c.4500+1G>T	NP_001107854.1:n.4500+1G>T
NM_001318827.2:c.4260+1G>T	NP_001305756.1:n.4260+1G>T
NM_001318829.2:c.4224+1G>T	NP_001305758.1:n.4224+1G>T
NM_001318831.2:c.3837+1G>T	NP_001305760.1:n.3837+1G>T
NM_001318832.2:c.4401+1G>T	NP_001305761.1:n.4401+1G>T
NM_001363528.2:c.4371+1G>T	NP_001350457.1:n.4371+1G>T
NM_021055.3:c.4440+1G>T	NP_066399.2:n.4440+1G>T