Canonical Allele Identifier: CA493043039

Gene: TSC2

Linked Data

• dbSNP Id: rs137854268
• MyVariant Identifiers: chr16:g.2131648G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2081647G>T , CM000678.2:g.2081647G>T	GRCh38
NC_000016.9:g.2131648G>T , CM000678.1:g.2131648G>T	GRCh37
NC_000016.8:g.2071649G>T	NCBI36
NG_005895.1:g.37342G>T , LRG_487:g.37342G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*2081G>T	ENSP00000455997.2:n.*2081G>T
ENST00000642206.2:c.3579G>T	ENSP00000495146.2:p.Ser1193=
ENST00000642365.2:c.3660G>T	ENSP00000495459.2:p.Ser1220=
ENST00000644417.2:c.*4112G>T	ENSP00000493912.2:n.*4112G>T
ENST00000646464.2:c.*4585G>T	ENSP00000496610.2:n.*4585G>T
ENST00000219476.9:c.3663G>T MANE Select	ENSP00000219476.3:p.Ser1221=
ENST00000350773.9:c.3663G>T	ENSP00000344383.4:p.Ser1221=
ENST00000401874.7:c.3531G>T	ENSP00000384468.2:p.Ser1177=
ENST00000568454.6:c.3564G>T	ENSP00000454487.1:p.Ser1188=
ENST00000642365.1:c.2317G>T
ENST00000642561.1:c.3534G>T	ENSP00000495099.1:p.Ser1178=
ENST00000642797.1:c.3534G>T	ENSP00000493846.1:p.Ser1178=
ENST00000642936.1:c.3531G>T	ENSP00000494514.1:p.Ser1177=
ENST00000643088.1:c.3531G>T	ENSP00000494747.1:p.Ser1177=
ENST00000643426.1:n.1311G>T
ENST00000643533.1:n.173G>T
ENST00000643946.1:c.3663G>T	ENSP00000495927.1:p.Ser1221=
ENST00000644043.1:c.3534G>T	ENSP00000496262.1:p.Ser1178=
ENST00000644329.1:c.3531G>T	ENSP00000496611.1:p.Ser1177=
ENST00000644335.1:c.3534G>T	ENSP00000496317.1:p.Ser1178=
ENST00000644399.1:c.3653G>T
ENST00000644722.1:n.809G>T
ENST00000645024.1:n.1816G>T
ENST00000646388.1:c.3663G>T	ENSP00000495921.1:p.Ser1221=
ENST00000646634.1:n.2547G>T
ENST00000646674.1:n.278G>T
ENST00000647042.1:n.955G>T
ENST00000647180.1:n.143G>T
ENST00000219476.7:c.3663G>T	ENSP00000219476.3:p.Ser1221=
ENST00000350773.8:c.3663G>T	ENSP00000344383.4:p.Ser1221=
ENST00000382538.10:c.3387G>T	ENSP00000371978.6:p.Ser1129=
ENST00000401874.6:c.3531G>T	ENSP00000384468.2:p.Ser1177=
ENST00000439117.6:c.*2830G>T	ENSP00000406980.2:n.*2830G>T
ENST00000439673.6:c.3423G>T	ENSP00000399232.2:p.Ser1141=
ENST00000497886.5:n.1490G>T
ENST00000568454.5:c.3564G>T	ENSP00000454487.1:p.Ser1188=
NM_000548.3:c.3663G>T , LRG_487t1:c.3663G>T	NP_000539.2:p.Ser1221=
NM_001077183.1:c.3531G>T	NP_001070651.1:p.Ser1177=
NM_001114382.1:c.3663G>T	NP_001107854.1:p.Ser1221=
XM_005255529.3:c.3534G>T	XP_005255586.2:p.Ser1178=
XM_005255531.3:c.3534G>T	XP_005255588.2:p.Ser1178=
XM_011522636.1:c.3663G>T	XP_011520938.1:p.Ser1221=
XM_011522637.1:c.3660G>T	XP_011520939.1:p.Ser1220=
XM_011522638.1:c.3552G>T	XP_011520940.1:p.Ser1184=
XM_011522639.1:c.3534G>T	XP_011520941.1:p.Ser1178=
XM_011522640.1:c.3531G>T	XP_011520942.1:p.Ser1177=
XM_011522641.1:c.3423G>T	XP_011520943.1:p.Ser1141=
NM_000548.4:c.3663G>T	NP_000539.2:p.Ser1221=
NM_001077183.2:c.3531G>T	NP_001070651.1:p.Ser1177=
NM_001114382.2:c.3663G>T	NP_001107854.1:p.Ser1221=
NM_001318827.1:c.3423G>T	NP_001305756.1:p.Ser1141=
NM_001318829.1:c.3387G>T	NP_001305758.1:p.Ser1129=
NM_001318831.1:c.2931G>T	NP_001305760.1:p.Ser977=
NM_001318832.1:c.3564G>T	NP_001305761.1:p.Ser1188=
NM_001363528.1:c.3534G>T	NP_001350457.1:p.Ser1178=
NM_021055.2:c.3534G>T	NP_066399.2:p.Ser1178=
XM_005255531.4:c.3534G>T	XP_005255588.2:p.Ser1178=
XM_011522636.2:c.3663G>T	XP_011520938.1:p.Ser1221=
XM_011522637.2:c.3660G>T	XP_011520939.1:p.Ser1220=
XM_011522638.2:c.3825G>T	XP_011520940.2:p.Ser1275=
XM_011522639.2:c.3534G>T	XP_011520941.1:p.Ser1178=
XM_011522640.2:c.3531G>T	XP_011520942.1:p.Ser1177=
XM_017023615.1:c.3660G>T	XP_016879104.1:p.Ser1220=
XM_017023616.1:c.3531G>T	XP_016879105.1:p.Ser1177=
XM_017023617.1:c.3696G>T	XP_016879106.1:p.Ser1232=
XM_017023618.1:c.2319G>T	XP_016879107.1:p.Ser773=
XM_024450413.1:c.3531G>T	XP_024306181.1:p.Ser1177=
NM_000548.5:c.3663G>T MANE Select	NP_000539.2:p.Ser1221=
NM_001370404.1:c.3531G>T	NP_001357333.1:p.Ser1177=
NM_001370405.1:c.3534G>T	NP_001357334.1:p.Ser1178=
NM_001077183.3:c.3531G>T	NP_001070651.1:p.Ser1177=
NM_001114382.3:c.3663G>T	NP_001107854.1:p.Ser1221=
NM_001318827.2:c.3423G>T	NP_001305756.1:p.Ser1141=
NM_001318829.2:c.3387G>T	NP_001305758.1:p.Ser1129=
NM_001318831.2:c.2931G>T	NP_001305760.1:p.Ser977=
NM_001318832.2:c.3564G>T	NP_001305761.1:p.Ser1188=
NM_001363528.2:c.3534G>T	NP_001350457.1:p.Ser1178=
NM_021055.3:c.3534G>T	NP_066399.2:p.Ser1178=