Canonical Allele Identifier: CA394289756

Gene: TSC2

Linked Data

• dbSNP Id: rs1555511663
• MyVariant Identifiers: chr16:g.2130378G>C (hg19) ; chr16:g.2080377G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2080377G>C , CM000678.2:g.2080377G>C	GRCh38
NC_000016.9:g.2130378G>C , CM000678.1:g.2130378G>C	GRCh37
NC_000016.8:g.2070379G>C	NCBI36
NG_005895.1:g.36072G>C , LRG_487:g.36072G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*2028G>C	ENSP00000455997.2:n.*2028G>C
ENST00000642206.2:c.3526G>C	ENSP00000495146.2:p.Gly1176Arg
ENST00000642365.2:c.3607G>C	ENSP00000495459.2:p.Gly1203Arg
ENST00000644417.2:c.*4059G>C	ENSP00000493912.2:n.*4059G>C
ENST00000646464.2:c.*4532G>C	ENSP00000496610.2:n.*4532G>C
ENST00000219476.9:c.3610G>C MANE Select	ENSP00000219476.3:p.Gly1204Arg
ENST00000350773.9:c.3610G>C	ENSP00000344383.4:p.Gly1204Arg
ENST00000401874.7:c.3478G>C	ENSP00000384468.2:p.Gly1160Arg
ENST00000568454.6:c.3511G>C	ENSP00000454487.1:p.Gly1171Arg
ENST00000642365.1:c.2264G>C
ENST00000642561.1:c.3481G>C	ENSP00000495099.1:p.Gly1161Arg
ENST00000642797.1:c.3481G>C	ENSP00000493846.1:p.Gly1161Arg
ENST00000642936.1:c.3478G>C	ENSP00000494514.1:p.Gly1160Arg
ENST00000643088.1:c.3478G>C	ENSP00000494747.1:p.Gly1160Arg
ENST00000643426.1:n.41G>C
ENST00000643946.1:c.3610G>C	ENSP00000495927.1:p.Gly1204Arg
ENST00000644043.1:c.3481G>C	ENSP00000496262.1:p.Gly1161Arg
ENST00000644329.1:c.3478G>C	ENSP00000496611.1:p.Gly1160Arg
ENST00000644335.1:c.3481G>C	ENSP00000496317.1:p.Gly1161Arg
ENST00000644399.1:c.3600G>C
ENST00000644722.1:n.756G>C
ENST00000645024.1:n.1763G>C
ENST00000646388.1:c.3610G>C	ENSP00000495921.1:p.Gly1204Arg
ENST00000646634.1:n.2494G>C
ENST00000646674.1:n.225G>C
ENST00000647042.1:n.902G>C
ENST00000647180.1:n.90G>C
ENST00000219476.7:c.3610G>C	ENSP00000219476.3:p.Gly1204Arg
ENST00000350773.8:c.3610G>C	ENSP00000344383.4:p.Gly1204Arg
ENST00000382538.10:c.3334G>C	ENSP00000371978.6:p.Gly1112Arg
ENST00000401874.6:c.3478G>C	ENSP00000384468.2:p.Gly1160Arg
ENST00000439117.6:c.*2777G>C	ENSP00000406980.2:n.*2777G>C
ENST00000439673.6:c.3370G>C	ENSP00000399232.2:p.Gly1124Arg
ENST00000497886.5:n.1437G>C
ENST00000568454.5:c.3511G>C	ENSP00000454487.1:p.Gly1171Arg
NM_000548.3:c.3610G>C , LRG_487t1:c.3610G>C	NP_000539.2:p.Gly1204Arg
NM_001077183.1:c.3478G>C	NP_001070651.1:p.Gly1160Arg
NM_001114382.1:c.3610G>C	NP_001107854.1:p.Gly1204Arg
XM_005255529.3:c.3481G>C	XP_005255586.2:p.Gly1161Arg
XM_005255531.3:c.3481G>C	XP_005255588.2:p.Gly1161Arg
XM_011522636.1:c.3610G>C	XP_011520938.1:p.Gly1204Arg
XM_011522637.1:c.3607G>C	XP_011520939.1:p.Gly1203Arg
XM_011522638.1:c.3499G>C	XP_011520940.1:p.Gly1167Arg
XM_011522639.1:c.3481G>C	XP_011520941.1:p.Gly1161Arg
XM_011522640.1:c.3478G>C	XP_011520942.1:p.Gly1160Arg
XM_011522641.1:c.3370G>C	XP_011520943.1:p.Gly1124Arg
NM_000548.4:c.3610G>C	NP_000539.2:p.Gly1204Arg
NM_001077183.2:c.3478G>C	NP_001070651.1:p.Gly1160Arg
NM_001114382.2:c.3610G>C	NP_001107854.1:p.Gly1204Arg
NM_001318827.1:c.3370G>C	NP_001305756.1:p.Gly1124Arg
NM_001318829.1:c.3334G>C	NP_001305758.1:p.Gly1112Arg
NM_001318831.1:c.2878G>C	NP_001305760.1:p.Gly960Arg
NM_001318832.1:c.3511G>C	NP_001305761.1:p.Gly1171Arg
NM_001363528.1:c.3481G>C	NP_001350457.1:p.Gly1161Arg
NM_021055.2:c.3481G>C	NP_066399.2:p.Gly1161Arg
XM_005255531.4:c.3481G>C	XP_005255588.2:p.Gly1161Arg
XM_011522636.2:c.3610G>C	XP_011520938.1:p.Gly1204Arg
XM_011522637.2:c.3607G>C	XP_011520939.1:p.Gly1203Arg
XM_011522638.2:c.3772G>C	XP_011520940.2:p.Gly1258Arg
XM_011522639.2:c.3481G>C	XP_011520941.1:p.Gly1161Arg
XM_011522640.2:c.3478G>C	XP_011520942.1:p.Gly1160Arg
XM_017023615.1:c.3607G>C	XP_016879104.1:p.Gly1203Arg
XM_017023616.1:c.3478G>C	XP_016879105.1:p.Gly1160Arg
XM_017023617.1:c.3643G>C	XP_016879106.1:p.Gly1215Arg
XM_017023618.1:c.2266G>C	XP_016879107.1:p.Gly756Arg
XM_024450413.1:c.3478G>C	XP_024306181.1:p.Gly1160Arg
NM_000548.5:c.3610G>C MANE Select	NP_000539.2:p.Gly1204Arg
NM_001370404.1:c.3478G>C	NP_001357333.1:p.Gly1160Arg
NM_001370405.1:c.3481G>C	NP_001357334.1:p.Gly1161Arg
NM_001077183.3:c.3478G>C	NP_001070651.1:p.Gly1160Arg
NM_001114382.3:c.3610G>C	NP_001107854.1:p.Gly1204Arg
NM_001318827.2:c.3370G>C	NP_001305756.1:p.Gly1124Arg
NM_001318829.2:c.3334G>C	NP_001305758.1:p.Gly1112Arg
NM_001318831.2:c.2878G>C	NP_001305760.1:p.Gly960Arg
NM_001318832.2:c.3511G>C	NP_001305761.1:p.Gly1171Arg
NM_001363528.2:c.3481G>C	NP_001350457.1:p.Gly1161Arg
NM_021055.3:c.3481G>C	NP_066399.2:p.Gly1161Arg