Canonical Allele Identifier: CA2838404741

Gene: TSC2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2079299dup , CM000678.2:g.2079299dup	GRCh38
NC_000016.9:g.2129300dup , CM000678.1:g.2129300dup	GRCh37
NC_000016.8:g.2069301dup	NCBI36
NG_005895.1:g.34994dup , LRG_487:g.34994dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*1573dup	ENSP00000455997.2:n.*1573dup
ENST00000642206.2:c.3071dup	ENSP00000495146.2:p.Ala1025SerfsTer?
ENST00000642365.2:c.3152dup	ENSP00000495459.2:p.Ala1052SerfsTer?
ENST00000644417.2:c.*3604dup	ENSP00000493912.2:n.*3604dup
ENST00000646464.2:c.*4077dup	ENSP00000496610.2:n.*4077dup
ENST00000219476.9:c.3155dup MANE Select	ENSP00000219476.3:p.Ala1053SerfsTer?
ENST00000350773.9:c.3155dup	ENSP00000344383.4:p.Ala1053SerfsTer?
ENST00000401874.7:c.3023dup	ENSP00000384468.2:p.Ala1009SerfsTer?
ENST00000471143.6:c.383dup	ENSP00000458541.2:n.383dup
ENST00000568366.6:n.512dup
ENST00000568454.6:c.3056dup	ENSP00000454487.1:p.Ala1020SerfsTer?
ENST00000642365.1:c.1809dup
ENST00000642561.1:c.3026dup	ENSP00000495099.1:p.Ala1010SerfsTer?
ENST00000642797.1:c.3026dup	ENSP00000493846.1:p.Ala1010SerfsTer?
ENST00000642936.1:c.3023dup	ENSP00000494514.1:p.Ala1009SerfsTer?
ENST00000643088.1:c.3023dup	ENSP00000494747.1:p.Ala1009SerfsTer?
ENST00000643946.1:c.3155dup	ENSP00000495927.1:p.Ala1053SerfsTer?
ENST00000644043.1:c.3026dup	ENSP00000496262.1:p.Ala1010SerfsTer?
ENST00000644329.1:c.3023dup	ENSP00000496611.1:p.Ala1009SerfsTer?
ENST00000644335.1:c.3026dup	ENSP00000496317.1:p.Ala1010SerfsTer?
ENST00000644399.1:c.3145dup
ENST00000644722.1:n.301dup
ENST00000645024.1:n.1308dup
ENST00000646388.1:c.3155dup	ENSP00000495921.1:p.Ala1053SerfsTer?
ENST00000646634.1:n.2039dup
ENST00000647042.1:n.447dup
ENST00000219476.7:c.3155dup	ENSP00000219476.3:p.Ala1053SerfsTer?
ENST00000350773.8:c.3155dup	ENSP00000344383.4:p.Ala1053SerfsTer?
ENST00000382538.10:c.2879dup	ENSP00000371978.6:p.Ala961SerfsTer?
ENST00000401874.6:c.3023dup	ENSP00000384468.2:p.Ala1009SerfsTer?
ENST00000439117.6:c.*2322dup	ENSP00000406980.2:n.*2322dup
ENST00000439673.6:c.2915dup	ENSP00000399232.2:p.Ala973SerfsTer?
ENST00000471143.5:c.381dup
ENST00000483020.5:c.395dup	ENSP00000460310.1:n.395dup
ENST00000497886.5:n.982dup
ENST00000561695.1:n.380dup
ENST00000568366.5:n.512dup
ENST00000568454.5:c.3056dup	ENSP00000454487.1:p.Ala1020SerfsTer?
NM_000548.3:c.3155dup , LRG_487t1:c.3155dup	NP_000539.2:p.Ala1053SerfsTer?
NM_001077183.1:c.3023dup	NP_001070651.1:p.Ala1009SerfsTer?
NM_001114382.1:c.3155dup	NP_001107854.1:p.Ala1053SerfsTer?
XM_005255529.3:c.3026dup	XP_005255586.2:p.Ala1010SerfsTer?
XM_005255531.3:c.3026dup	XP_005255588.2:p.Ala1010SerfsTer?
XM_011522636.1:c.3155dup	XP_011520938.1:p.Ala1053SerfsTer?
XM_011522637.1:c.3152dup	XP_011520939.1:p.Ala1052SerfsTer?
XM_011522638.1:c.3044dup	XP_011520940.1:p.Ala1016SerfsTer?
XM_011522639.1:c.3026dup	XP_011520941.1:p.Ala1010SerfsTer?
XM_011522640.1:c.3023dup	XP_011520942.1:p.Ala1009SerfsTer?
XM_011522641.1:c.2915dup	XP_011520943.1:p.Ala973SerfsTer?
NM_000548.4:c.3155dup	NP_000539.2:p.Ala1053SerfsTer?
NM_001077183.2:c.3023dup	NP_001070651.1:p.Ala1009SerfsTer?
NM_001114382.2:c.3155dup	NP_001107854.1:p.Ala1053SerfsTer?
NM_001318827.1:c.2915dup	NP_001305756.1:p.Ala973SerfsTer?
NM_001318829.1:c.2879dup	NP_001305758.1:p.Ala961SerfsTer?
NM_001318831.1:c.2423dup	NP_001305760.1:p.Ala809SerfsTer?
NM_001318832.1:c.3056dup	NP_001305761.1:p.Ala1020SerfsTer?
NM_001363528.1:c.3026dup	NP_001350457.1:p.Ala1010SerfsTer?
NM_021055.2:c.3026dup	NP_066399.2:p.Ala1010SerfsTer?
XM_005255531.4:c.3026dup	XP_005255588.2:p.Ala1010SerfsTer?
XM_011522636.2:c.3155dup	XP_011520938.1:p.Ala1053SerfsTer?
XM_011522637.2:c.3152dup	XP_011520939.1:p.Ala1052SerfsTer?
XM_011522638.2:c.3317dup	XP_011520940.2:p.Ala1107SerfsTer?
XM_011522639.2:c.3026dup	XP_011520941.1:p.Ala1010SerfsTer?
XM_011522640.2:c.3023dup	XP_011520942.1:p.Ala1009SerfsTer?
XM_017023615.1:c.3152dup	XP_016879104.1:p.Ala1052SerfsTer?
XM_017023616.1:c.3023dup	XP_016879105.1:p.Ala1009SerfsTer?
XM_017023617.1:c.3188dup	XP_016879106.1:p.Ala1064SerfsTer?
XM_017023618.1:c.1811dup	XP_016879107.1:p.Ala605SerfsTer?
XM_024450413.1:c.3023dup	XP_024306181.1:p.Ala1009SerfsTer?
NM_000548.5:c.3155dup MANE Select	NP_000539.2:p.Ala1053SerfsTer?
NM_001370404.1:c.3023dup	NP_001357333.1:p.Ala1009SerfsTer?
NM_001370405.1:c.3026dup	NP_001357334.1:p.Ala1010SerfsTer?
NM_001077183.3:c.3023dup	NP_001070651.1:p.Ala1009SerfsTer?
NM_001114382.3:c.3155dup	NP_001107854.1:p.Ala1053SerfsTer?
NM_001318827.2:c.2915dup	NP_001305756.1:p.Ala973SerfsTer?
NM_001318829.2:c.2879dup	NP_001305758.1:p.Ala961SerfsTer?
NM_001318831.2:c.2423dup	NP_001305760.1:p.Ala809SerfsTer?
NM_001318832.2:c.3056dup	NP_001305761.1:p.Ala1020SerfsTer?
NM_001363528.2:c.3026dup	NP_001350457.1:p.Ala1010SerfsTer?
NM_021055.3:c.3026dup	NP_066399.2:p.Ala1010SerfsTer?