Canonical Allele Identifier: CA493042969

Gene: TSC2

Linked Data

• ClinVar Variation Id: 1115814
• ClinVar RCV Id: RCV001443968
• dbSNP Id: rs1057522260
• MyVariant Identifiers: chr16:g.2131603C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2081602C>A , CM000678.2:g.2081602C>A	GRCh38
NC_000016.9:g.2131603C>A , CM000678.1:g.2131603C>A	GRCh37
NC_000016.8:g.2071604C>A	NCBI36
NG_005895.1:g.37297C>A , LRG_487:g.37297C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*2036C>A	ENSP00000455997.2:n.*2036C>A
ENST00000642206.2:c.3534C>A	ENSP00000495146.2:p.Thr1178=
ENST00000642365.2:c.3615C>A	ENSP00000495459.2:p.Thr1205=
ENST00000644417.2:c.*4067C>A	ENSP00000493912.2:n.*4067C>A
ENST00000646464.2:c.*4540C>A	ENSP00000496610.2:n.*4540C>A
ENST00000219476.9:c.3618C>A MANE Select	ENSP00000219476.3:p.Thr1206=
ENST00000350773.9:c.3618C>A	ENSP00000344383.4:p.Thr1206=
ENST00000401874.7:c.3486C>A	ENSP00000384468.2:p.Thr1162=
ENST00000568454.6:c.3519C>A	ENSP00000454487.1:p.Thr1173=
ENST00000642365.1:c.2272C>A
ENST00000642561.1:c.3489C>A	ENSP00000495099.1:p.Thr1163=
ENST00000642797.1:c.3489C>A	ENSP00000493846.1:p.Thr1163=
ENST00000642936.1:c.3486C>A	ENSP00000494514.1:p.Thr1162=
ENST00000643088.1:c.3486C>A	ENSP00000494747.1:p.Thr1162=
ENST00000643426.1:n.1266C>A
ENST00000643533.1:n.128C>A
ENST00000643946.1:c.3618C>A	ENSP00000495927.1:p.Thr1206=
ENST00000644043.1:c.3489C>A	ENSP00000496262.1:p.Thr1163=
ENST00000644329.1:c.3486C>A	ENSP00000496611.1:p.Thr1162=
ENST00000644335.1:c.3489C>A	ENSP00000496317.1:p.Thr1163=
ENST00000644399.1:c.3608C>A
ENST00000644722.1:n.764C>A
ENST00000645024.1:n.1771C>A
ENST00000646388.1:c.3618C>A	ENSP00000495921.1:p.Thr1206=
ENST00000646634.1:n.2502C>A
ENST00000646674.1:n.233C>A
ENST00000647042.1:n.910C>A
ENST00000647180.1:n.98C>A
ENST00000219476.7:c.3618C>A	ENSP00000219476.3:p.Thr1206=
ENST00000350773.8:c.3618C>A	ENSP00000344383.4:p.Thr1206=
ENST00000382538.10:c.3342C>A	ENSP00000371978.6:p.Thr1114=
ENST00000401874.6:c.3486C>A	ENSP00000384468.2:p.Thr1162=
ENST00000439117.6:c.*2785C>A	ENSP00000406980.2:n.*2785C>A
ENST00000439673.6:c.3378C>A	ENSP00000399232.2:p.Thr1126=
ENST00000497886.5:n.1445C>A
ENST00000568454.5:c.3519C>A	ENSP00000454487.1:p.Thr1173=
NM_000548.3:c.3618C>A , LRG_487t1:c.3618C>A	NP_000539.2:p.Thr1206=
NM_001077183.1:c.3486C>A	NP_001070651.1:p.Thr1162=
NM_001114382.1:c.3618C>A	NP_001107854.1:p.Thr1206=
XM_005255529.3:c.3489C>A	XP_005255586.2:p.Thr1163=
XM_005255531.3:c.3489C>A	XP_005255588.2:p.Thr1163=
XM_011522636.1:c.3618C>A	XP_011520938.1:p.Thr1206=
XM_011522637.1:c.3615C>A	XP_011520939.1:p.Thr1205=
XM_011522638.1:c.3507C>A	XP_011520940.1:p.Thr1169=
XM_011522639.1:c.3489C>A	XP_011520941.1:p.Thr1163=
XM_011522640.1:c.3486C>A	XP_011520942.1:p.Thr1162=
XM_011522641.1:c.3378C>A	XP_011520943.1:p.Thr1126=
NM_000548.4:c.3618C>A	NP_000539.2:p.Thr1206=
NM_001077183.2:c.3486C>A	NP_001070651.1:p.Thr1162=
NM_001114382.2:c.3618C>A	NP_001107854.1:p.Thr1206=
NM_001318827.1:c.3378C>A	NP_001305756.1:p.Thr1126=
NM_001318829.1:c.3342C>A	NP_001305758.1:p.Thr1114=
NM_001318831.1:c.2886C>A	NP_001305760.1:p.Thr962=
NM_001318832.1:c.3519C>A	NP_001305761.1:p.Thr1173=
NM_001363528.1:c.3489C>A	NP_001350457.1:p.Thr1163=
NM_021055.2:c.3489C>A	NP_066399.2:p.Thr1163=
XM_005255531.4:c.3489C>A	XP_005255588.2:p.Thr1163=
XM_011522636.2:c.3618C>A	XP_011520938.1:p.Thr1206=
XM_011522637.2:c.3615C>A	XP_011520939.1:p.Thr1205=
XM_011522638.2:c.3780C>A	XP_011520940.2:p.Thr1260=
XM_011522639.2:c.3489C>A	XP_011520941.1:p.Thr1163=
XM_011522640.2:c.3486C>A	XP_011520942.1:p.Thr1162=
XM_017023615.1:c.3615C>A	XP_016879104.1:p.Thr1205=
XM_017023616.1:c.3486C>A	XP_016879105.1:p.Thr1162=
XM_017023617.1:c.3651C>A	XP_016879106.1:p.Thr1217=
XM_017023618.1:c.2274C>A	XP_016879107.1:p.Thr758=
XM_024450413.1:c.3486C>A	XP_024306181.1:p.Thr1162=
NM_000548.5:c.3618C>A MANE Select	NP_000539.2:p.Thr1206=
NM_001370404.1:c.3486C>A	NP_001357333.1:p.Thr1162=
NM_001370405.1:c.3489C>A	NP_001357334.1:p.Thr1163=
NM_001077183.3:c.3486C>A	NP_001070651.1:p.Thr1162=
NM_001114382.3:c.3618C>A	NP_001107854.1:p.Thr1206=
NM_001318827.2:c.3378C>A	NP_001305756.1:p.Thr1126=
NM_001318829.2:c.3342C>A	NP_001305758.1:p.Thr1114=
NM_001318831.2:c.2886C>A	NP_001305760.1:p.Thr962=
NM_001318832.2:c.3519C>A	NP_001305761.1:p.Thr1173=
NM_001363528.2:c.3489C>A	NP_001350457.1:p.Thr1163=
NM_021055.3:c.3489C>A	NP_066399.2:p.Thr1163=