Canonical Allele Identifier: CA394272876

Gene: TSC2

Linked Data

• ClinVar Variation Id: 1779692
• ClinVar RCV Id: RCV002401747 ; RCV003512176
• dbSNP Id: rs796053487
• MyVariant Identifiers: chr16:g.2120506T>C (hg19) ; chr16:g.2070505T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2070505T>C , CM000678.2:g.2070505T>C	GRCh38
NC_000016.9:g.2120506T>C , CM000678.1:g.2120506T>C	GRCh37
NC_000016.8:g.2060507T>C	NCBI36
NG_005895.1:g.26200T>C , LRG_487:g.26200T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*313T>C	ENSP00000455997.2:n.*313T>C
ENST00000642206.2:c.1811T>C	ENSP00000495146.2:p.Met604Thr
ENST00000642365.2:c.1766T>C	ENSP00000495459.2:p.Met589Thr
ENST00000644417.2:c.*1203T>C	ENSP00000493912.2:n.*1203T>C
ENST00000646464.2:c.*1371T>C	ENSP00000496610.2:n.*1371T>C
ENST00000219476.9:c.1766T>C MANE Select	ENSP00000219476.3:p.Met589Thr
ENST00000350773.9:c.1766T>C	ENSP00000344383.4:p.Met589Thr
ENST00000401874.7:c.1766T>C	ENSP00000384468.2:p.Met589Thr
ENST00000568454.6:c.1799T>C	ENSP00000454487.1:p.Met600Thr
ENST00000642365.1:c.423T>C
ENST00000642561.1:c.1766T>C	ENSP00000495099.1:p.Met589Thr
ENST00000642797.1:c.1766T>C	ENSP00000493846.1:p.Met589Thr
ENST00000642936.1:c.1766T>C	ENSP00000494514.1:p.Met589Thr
ENST00000643088.1:c.1766T>C	ENSP00000494747.1:p.Met589Thr
ENST00000643298.1:c.*1268T>C	ENSP00000494393.1:n.*1268T>C
ENST00000643946.1:c.1766T>C	ENSP00000495927.1:p.Met589Thr
ENST00000644043.1:c.1766T>C	ENSP00000496262.1:p.Met589Thr
ENST00000644135.1:c.*266T>C	ENSP00000495644.1:n.*266T>C
ENST00000644329.1:c.1766T>C	ENSP00000496611.1:p.Met589Thr
ENST00000644335.1:c.1766T>C	ENSP00000496317.1:p.Met589Thr
ENST00000644399.1:c.1759T>C
ENST00000644847.1:n.758T>C
ENST00000645552.1:n.46T>C
ENST00000646388.1:c.1766T>C	ENSP00000495921.1:p.Met589Thr
ENST00000646634.1:n.779T>C
ENST00000219476.7:c.1766T>C	ENSP00000219476.3:p.Met589Thr
ENST00000350773.8:c.1766T>C	ENSP00000344383.4:p.Met589Thr
ENST00000382538.10:c.1619T>C	ENSP00000371978.6:p.Met540Thr
ENST00000401874.6:c.1766T>C	ENSP00000384468.2:p.Met589Thr
ENST00000439117.6:c.*1065T>C	ENSP00000406980.2:n.*1065T>C
ENST00000439673.6:c.1655T>C	ENSP00000399232.2:p.Met552Thr
ENST00000488675.5:n.273T>C
ENST00000562474.1:n.491T>C
ENST00000568454.5:c.1799T>C	ENSP00000454487.1:p.Met600Thr
ENST00000568566.5:c.406T>C	ENSP00000455997.1:n.406T>C
NM_000548.3:c.1766T>C , LRG_487t1:c.1766T>C	NP_000539.2:p.Met589Thr
NM_001077183.1:c.1766T>C	NP_001070651.1:p.Met589Thr
NM_001114382.1:c.1766T>C	NP_001107854.1:p.Met589Thr
XM_005255529.3:c.1766T>C	XP_005255586.2:p.Met589Thr
XM_005255531.3:c.1766T>C	XP_005255588.2:p.Met589Thr
XM_011522636.1:c.1766T>C	XP_011520938.1:p.Met589Thr
XM_011522637.1:c.1766T>C	XP_011520939.1:p.Met589Thr
XM_011522638.1:c.1655T>C	XP_011520940.1:p.Met552Thr
XM_011522639.1:c.1766T>C	XP_011520941.1:p.Met589Thr
XM_011522640.1:c.1766T>C	XP_011520942.1:p.Met589Thr
XM_011522641.1:c.1655T>C	XP_011520943.1:p.Met552Thr
NM_000548.4:c.1766T>C	NP_000539.2:p.Met589Thr
NM_001077183.2:c.1766T>C	NP_001070651.1:p.Met589Thr
NM_001114382.2:c.1766T>C	NP_001107854.1:p.Met589Thr
NM_001318827.1:c.1655T>C	NP_001305756.1:p.Met552Thr
NM_001318829.1:c.1619T>C	NP_001305758.1:p.Met540Thr
NM_001318831.1:c.1166T>C	NP_001305760.1:p.Met389Thr
NM_001318832.1:c.1799T>C	NP_001305761.1:p.Met600Thr
NM_001363528.1:c.1766T>C	NP_001350457.1:p.Met589Thr
NM_021055.2:c.1766T>C	NP_066399.2:p.Met589Thr
XM_005255531.4:c.1766T>C	XP_005255588.2:p.Met589Thr
XM_011522636.2:c.1766T>C	XP_011520938.1:p.Met589Thr
XM_011522637.2:c.1766T>C	XP_011520939.1:p.Met589Thr
XM_011522638.2:c.1928T>C	XP_011520940.2:p.Met643Thr
XM_011522639.2:c.1766T>C	XP_011520941.1:p.Met589Thr
XM_011522640.2:c.1766T>C	XP_011520942.1:p.Met589Thr
XM_017023615.1:c.1766T>C	XP_016879104.1:p.Met589Thr
XM_017023616.1:c.1766T>C	XP_016879105.1:p.Met589Thr
XM_017023617.1:c.1928T>C	XP_016879106.1:p.Met643Thr
XM_017023618.1:c.422T>C	XP_016879107.1:p.Met141Thr
XM_024450413.1:c.1766T>C	XP_024306181.1:p.Met589Thr
NM_000548.5:c.1766T>C MANE Select	NP_000539.2:p.Met589Thr
NM_001370404.1:c.1766T>C	NP_001357333.1:p.Met589Thr
NM_001370405.1:c.1766T>C	NP_001357334.1:p.Met589Thr
NM_001077183.3:c.1766T>C	NP_001070651.1:p.Met589Thr
NM_001114382.3:c.1766T>C	NP_001107854.1:p.Met589Thr
NM_001318827.2:c.1655T>C	NP_001305756.1:p.Met552Thr
NM_001318829.2:c.1619T>C	NP_001305758.1:p.Met540Thr
NM_001318831.2:c.1166T>C	NP_001305760.1:p.Met389Thr
NM_001318832.2:c.1799T>C	NP_001305761.1:p.Met600Thr
NM_001363528.2:c.1766T>C	NP_001350457.1:p.Met589Thr
NM_021055.3:c.1766T>C	NP_066399.2:p.Met589Thr