Canonical Allele Identifier: CA019809

Gene: TSC2

Linked Data

• ClinVar Variation Id: 49778
• ClinVar RCV Id: RCV000043043 ; RCV001171696 ; RCV001377312
• dbSNP Id: rs45517324
• MyVariant Identifiers: chr16:g.2133818G>T (hg19) ; chr16:g.2083817G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2083817G>T , CM000678.2:g.2083817G>T	GRCh38
NC_000016.9:g.2133818G>T , CM000678.1:g.2133818G>T	GRCh37
NC_000016.8:g.2073819G>T	NCBI36
NG_005895.1:g.39512G>T , LRG_487:g.39512G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*2354+1G>T	ENSP00000455997.2:n.*2354+1G>T
ENST00000642206.2:c.3852+1G>T	ENSP00000495146.2:n.3852+1G>T
ENST00000642365.2:c.4002+1G>T	ENSP00000495459.2:n.4002+1G>T
ENST00000644417.2:c.*4385+1G>T	ENSP00000493912.2:n.*4385+1G>T
ENST00000646464.2:c.*6754+1G>T	ENSP00000496610.2:n.*6754+1G>T
ENST00000219476.9:c.4005+1G>T MANE Select	ENSP00000219476.3:n.4005+1G>T
ENST00000350773.9:c.3936+1G>T	ENSP00000344383.4:n.3936+1G>T
ENST00000401874.7:c.3804+1G>T	ENSP00000384468.2:n.3804+1G>T
ENST00000568454.6:c.3837+1G>T	ENSP00000454487.1:n.3837+1G>T
ENST00000569110.2:c.241+1G>T
ENST00000569930.2:n.1887+1G>T
ENST00000642365.1:c.2659+1G>T
ENST00000642561.1:c.3876+1G>T	ENSP00000495099.1:n.3876+1G>T
ENST00000642728.1:n.187+1G>T
ENST00000642797.1:c.3807+1G>T	ENSP00000493846.1:n.3807+1G>T
ENST00000642936.1:c.3873+1G>T	ENSP00000494514.1:n.3873+1G>T
ENST00000643088.1:c.3804+1G>T	ENSP00000494747.1:n.3804+1G>T
ENST00000643177.1:n.19+1G>T
ENST00000643426.1:n.1653+1G>T
ENST00000643533.1:n.446+1G>T
ENST00000643946.1:c.3936+1G>T	ENSP00000495927.1:n.3936+1G>T
ENST00000644043.1:c.3876+1G>T	ENSP00000496262.1:n.3876+1G>T
ENST00000644329.1:c.3804+1G>T	ENSP00000496611.1:n.3804+1G>T
ENST00000644335.1:c.3807+1G>T	ENSP00000496317.1:n.3807+1G>T
ENST00000644399.1:c.3926+1G>T
ENST00000645024.1:n.2089+1G>T
ENST00000645186.1:c.248+1G>T
ENST00000646388.1:c.4005+1G>T	ENSP00000495921.1:n.4005+1G>T
ENST00000646634.1:n.2820+1G>T
ENST00000646674.1:n.1257+1G>T
ENST00000647042.1:n.1228+1G>T
ENST00000647180.1:n.1118+1G>T
ENST00000219476.7:c.4005+1G>T	ENSP00000219476.3:n.4005+1G>T
ENST00000350773.8:c.3936+1G>T	ENSP00000344383.4:n.3936+1G>T
ENST00000382538.10:c.3660+1G>T	ENSP00000371978.6:n.3660+1G>T
ENST00000401874.6:c.3804+1G>T	ENSP00000384468.2:n.3804+1G>T
ENST00000439117.6:c.*3172+1G>T	ENSP00000406980.2:n.*3172+1G>T
ENST00000439673.6:c.3696+1G>T	ENSP00000399232.2:n.3696+1G>T
ENST00000497886.5:n.1763+1G>T
ENST00000568454.5:c.3837+1G>T	ENSP00000454487.1:n.3837+1G>T
ENST00000569110.1:c.187+1G>T
ENST00000569930.1:n.1120+1G>T
NM_000548.3:c.4005+1G>T , LRG_487t1:c.4005+1G>T	NP_000539.2:n.4005+1G>T
NM_001077183.1:c.3804+1G>T	NP_001070651.1:n.3804+1G>T
NM_001114382.1:c.3936+1G>T	NP_001107854.1:n.3936+1G>T
XM_005255529.3:c.3876+1G>T	XP_005255586.2:n.3876+1G>T
XM_005255531.3:c.3807+1G>T	XP_005255588.2:n.3807+1G>T
XM_011522636.1:c.4059+1G>T	XP_011520938.1:n.4059+1G>T
XM_011522637.1:c.4056+1G>T	XP_011520939.1:n.4056+1G>T
XM_011522638.1:c.3948+1G>T	XP_011520940.1:n.3948+1G>T
XM_011522639.1:c.3930+1G>T	XP_011520941.1:n.3930+1G>T
XM_011522640.1:c.3927+1G>T	XP_011520942.1:n.3927+1G>T
XM_011522641.1:c.3696+1G>T	XP_011520943.1:n.3696+1G>T
NM_000548.4:c.4005+1G>T	NP_000539.2:n.4005+1G>T
NM_001077183.2:c.3804+1G>T	NP_001070651.1:n.3804+1G>T
NM_001114382.2:c.3936+1G>T	NP_001107854.1:n.3936+1G>T
NM_001318827.1:c.3696+1G>T	NP_001305756.1:n.3696+1G>T
NM_001318829.1:c.3660+1G>T	NP_001305758.1:n.3660+1G>T
NM_001318831.1:c.3273+1G>T	NP_001305760.1:n.3273+1G>T
NM_001318832.1:c.3837+1G>T	NP_001305761.1:n.3837+1G>T
NM_001363528.1:c.3807+1G>T	NP_001350457.1:n.3807+1G>T
NM_021055.2:c.3876+1G>T	NP_066399.2:n.3876+1G>T
XM_005255531.4:c.3807+1G>T	XP_005255588.2:n.3807+1G>T
XM_011522636.2:c.4059+1G>T	XP_011520938.1:n.4059+1G>T
XM_011522637.2:c.4056+1G>T	XP_011520939.1:n.4056+1G>T
XM_011522638.2:c.4221+1G>T	XP_011520940.2:n.4221+1G>T
XM_011522639.2:c.3930+1G>T	XP_011520941.1:n.3930+1G>T
XM_011522640.2:c.3927+1G>T	XP_011520942.1:n.3927+1G>T
XM_017023615.1:c.4002+1G>T	XP_016879104.1:n.4002+1G>T
XM_017023616.1:c.3873+1G>T	XP_016879105.1:n.3873+1G>T
XM_017023617.1:c.3969+1G>T	XP_016879106.1:n.3969+1G>T
XM_017023618.1:c.2715+1G>T	XP_016879107.1:n.2715+1G>T
XM_024450413.1:c.3804+1G>T	XP_024306181.1:n.3804+1G>T
NM_000548.5:c.4005+1G>T MANE Select	NP_000539.2:n.4005+1G>T
NM_001370404.1:c.3873+1G>T	NP_001357333.1:n.3873+1G>T
NM_001370405.1:c.3876+1G>T	NP_001357334.1:n.3876+1G>T
NM_001077183.3:c.3804+1G>T	NP_001070651.1:n.3804+1G>T
NM_001114382.3:c.3936+1G>T	NP_001107854.1:n.3936+1G>T
NM_001318827.2:c.3696+1G>T	NP_001305756.1:n.3696+1G>T
NM_001318829.2:c.3660+1G>T	NP_001305758.1:n.3660+1G>T
NM_001318831.2:c.3273+1G>T	NP_001305760.1:n.3273+1G>T
NM_001318832.2:c.3837+1G>T	NP_001305761.1:n.3837+1G>T
NM_001363528.2:c.3807+1G>T	NP_001350457.1:n.3807+1G>T
NM_021055.3:c.3876+1G>T	NP_066399.2:n.3876+1G>T