Canonical Allele Identifier: CA044546

Gene: TSC2

Linked Data

• dbSNP Id: rs774008119
• ExAC: 16:2129281 C / G
• gnomAD v2: 16-2129281-C-G
• MyVariant Identifiers: chr16:g.2129281C>G (hg19) ; chr16:g.2079280C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2079280C>G , CM000678.2:g.2079280C>G	GRCh38
NC_000016.9:g.2129281C>G , CM000678.1:g.2129281C>G	GRCh37
NC_000016.8:g.2069282C>G	NCBI36
NG_005895.1:g.34975C>G , LRG_487:g.34975C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*1554C>G	ENSP00000455997.2:n.*1554C>G
ENST00000642206.2:c.3052C>G	ENSP00000495146.2:p.Pro1018Ala
ENST00000642365.2:c.3133C>G	ENSP00000495459.2:p.Pro1045Ala
ENST00000644417.2:c.*3585C>G	ENSP00000493912.2:n.*3585C>G
ENST00000646464.2:c.*4058C>G	ENSP00000496610.2:n.*4058C>G
ENST00000219476.9:c.3136C>G MANE Select	ENSP00000219476.3:p.Pro1046Ala
ENST00000350773.9:c.3136C>G	ENSP00000344383.4:p.Pro1046Ala
ENST00000401874.7:c.3004C>G	ENSP00000384468.2:p.Pro1002Ala
ENST00000471143.6:c.364C>G	ENSP00000458541.2:n.364C>G
ENST00000568366.6:n.493C>G
ENST00000568454.6:c.3037C>G	ENSP00000454487.1:p.Pro1013Ala
ENST00000642365.1:c.1790C>G
ENST00000642561.1:c.3007C>G	ENSP00000495099.1:p.Pro1003Ala
ENST00000642797.1:c.3007C>G	ENSP00000493846.1:p.Pro1003Ala
ENST00000642936.1:c.3004C>G	ENSP00000494514.1:p.Pro1002Ala
ENST00000643088.1:c.3004C>G	ENSP00000494747.1:p.Pro1002Ala
ENST00000643946.1:c.3136C>G	ENSP00000495927.1:p.Pro1046Ala
ENST00000644043.1:c.3007C>G	ENSP00000496262.1:p.Pro1003Ala
ENST00000644329.1:c.3004C>G	ENSP00000496611.1:p.Pro1002Ala
ENST00000644335.1:c.3007C>G	ENSP00000496317.1:p.Pro1003Ala
ENST00000644399.1:c.3126C>G
ENST00000644722.1:n.282C>G
ENST00000645024.1:n.1289C>G
ENST00000646388.1:c.3136C>G	ENSP00000495921.1:p.Pro1046Ala
ENST00000646634.1:n.2020C>G
ENST00000647042.1:n.428C>G
ENST00000219476.7:c.3136C>G	ENSP00000219476.3:p.Pro1046Ala
ENST00000350773.8:c.3136C>G	ENSP00000344383.4:p.Pro1046Ala
ENST00000382538.10:c.2860C>G	ENSP00000371978.6:p.Pro954Ala
ENST00000401874.6:c.3004C>G	ENSP00000384468.2:p.Pro1002Ala
ENST00000439117.6:c.*2303C>G	ENSP00000406980.2:n.*2303C>G
ENST00000439673.6:c.2896C>G	ENSP00000399232.2:p.Pro966Ala
ENST00000471143.5:c.362C>G
ENST00000483020.5:c.376C>G	ENSP00000460310.1:n.376C>G
ENST00000497886.5:n.963C>G
ENST00000561695.1:n.361C>G
ENST00000568366.5:n.493C>G
ENST00000568454.5:c.3037C>G	ENSP00000454487.1:p.Pro1013Ala
NM_000548.3:c.3136C>G , LRG_487t1:c.3136C>G	NP_000539.2:p.Pro1046Ala
NM_001077183.1:c.3004C>G	NP_001070651.1:p.Pro1002Ala
NM_001114382.1:c.3136C>G	NP_001107854.1:p.Pro1046Ala
XM_005255529.3:c.3007C>G	XP_005255586.2:p.Pro1003Ala
XM_005255531.3:c.3007C>G	XP_005255588.2:p.Pro1003Ala
XM_011522636.1:c.3136C>G	XP_011520938.1:p.Pro1046Ala
XM_011522637.1:c.3133C>G	XP_011520939.1:p.Pro1045Ala
XM_011522638.1:c.3025C>G	XP_011520940.1:p.Pro1009Ala
XM_011522639.1:c.3007C>G	XP_011520941.1:p.Pro1003Ala
XM_011522640.1:c.3004C>G	XP_011520942.1:p.Pro1002Ala
XM_011522641.1:c.2896C>G	XP_011520943.1:p.Pro966Ala
NM_000548.4:c.3136C>G	NP_000539.2:p.Pro1046Ala
NM_001077183.2:c.3004C>G	NP_001070651.1:p.Pro1002Ala
NM_001114382.2:c.3136C>G	NP_001107854.1:p.Pro1046Ala
NM_001318827.1:c.2896C>G	NP_001305756.1:p.Pro966Ala
NM_001318829.1:c.2860C>G	NP_001305758.1:p.Pro954Ala
NM_001318831.1:c.2404C>G	NP_001305760.1:p.Pro802Ala
NM_001318832.1:c.3037C>G	NP_001305761.1:p.Pro1013Ala
NM_001363528.1:c.3007C>G	NP_001350457.1:p.Pro1003Ala
NM_021055.2:c.3007C>G	NP_066399.2:p.Pro1003Ala
XM_005255531.4:c.3007C>G	XP_005255588.2:p.Pro1003Ala
XM_011522636.2:c.3136C>G	XP_011520938.1:p.Pro1046Ala
XM_011522637.2:c.3133C>G	XP_011520939.1:p.Pro1045Ala
XM_011522638.2:c.3298C>G	XP_011520940.2:p.Pro1100Ala
XM_011522639.2:c.3007C>G	XP_011520941.1:p.Pro1003Ala
XM_011522640.2:c.3004C>G	XP_011520942.1:p.Pro1002Ala
XM_017023615.1:c.3133C>G	XP_016879104.1:p.Pro1045Ala
XM_017023616.1:c.3004C>G	XP_016879105.1:p.Pro1002Ala
XM_017023617.1:c.3169C>G	XP_016879106.1:p.Pro1057Ala
XM_017023618.1:c.1792C>G	XP_016879107.1:p.Pro598Ala
XM_024450413.1:c.3004C>G	XP_024306181.1:p.Pro1002Ala
NM_000548.5:c.3136C>G MANE Select	NP_000539.2:p.Pro1046Ala
NM_001370404.1:c.3004C>G	NP_001357333.1:p.Pro1002Ala
NM_001370405.1:c.3007C>G	NP_001357334.1:p.Pro1003Ala
NM_001077183.3:c.3004C>G	NP_001070651.1:p.Pro1002Ala
NM_001114382.3:c.3136C>G	NP_001107854.1:p.Pro1046Ala
NM_001318827.2:c.2896C>G	NP_001305756.1:p.Pro966Ala
NM_001318829.2:c.2860C>G	NP_001305758.1:p.Pro954Ala
NM_001318831.2:c.2404C>G	NP_001305760.1:p.Pro802Ala
NM_001318832.2:c.3037C>G	NP_001305761.1:p.Pro1013Ala
NM_001363528.2:c.3007C>G	NP_001350457.1:p.Pro1003Ala
NM_021055.3:c.3007C>G	NP_066399.2:p.Pro1003Ala