Canonical Allele Identifier: CA1882417498

Gene: TSC1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132911462_132911469delinsTTCAGTTA , CM000671.2:g.132911462_132911469delinsTTCAGTTA	GRCh38
NC_000009.11:g.135786849_135786856delinsTTCAGTTA , CM000671.1:g.135786849_135786856delinsTTCAGTTA	GRCh37
NC_000009.10:g.134776670_134776677delinsTTCAGTTA	NCBI36
NG_012386.1:g.38165_38172delinsTAACTGAA , LRG_486:g.38165_38172delinsTAACTGAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000475903.7:c.1013_1020delinsTAACTGAA	ENSP00000496126.2:p.Ile338=
ENST00000490179.4:c.1013_1020delinsTAACTGAA	ENSP00000495533.2:p.Ile338=
ENST00000642261.2:c.1013_1020delinsTAACTGAA	ENSP00000494743.2:p.Ile338=
ENST00000643275.2:c.1013_1020delinsTAACTGAA	ENSP00000495598.2:p.Ile338=
ENST00000643362.2:c.860_867delinsTAACTGAA	ENSP00000496398.2:p.Ile287=
ENST00000643625.2:c.1013_1020delinsTAACTGAA	ENSP00000495546.2:p.Ile338=
ENST00000643691.2:c.650_657delinsTAACTGAA	ENSP00000494916.2:p.Ile217=
ENST00000644184.2:c.1013_1020delinsTAACTGAA	ENSP00000495428.2:p.Ile338=
ENST00000645129.2:c.860_867delinsTAACTGAA	ENSP00000493639.2:p.Ile287=
ENST00000646440.2:c.1013_1020delinsTAACTGAA	ENSP00000495830.2:p.Ile338=
ENST00000647078.2:c.1013_1020delinsTAACTGAA	ENSP00000496066.1:p.Ile338=
ENST00000298552.9:c.1013_1020delinsTAACTGAA MANE Select	ENSP00000298552.3:p.Ile338=
ENST00000403810.6:c.1013_1020delinsTAACTGAA	ENSP00000386093.1:p.Ile338=
ENST00000493467.6:n.287_294delinsTAACTGAA
ENST00000642344.1:c.*754_*761delinsTAACTGAA	ENSP00000494847.1:n.*754_*761delinsTAACTG...
ENST00000642617.1:c.1013_1020delinsTAACTGAA	ENSP00000493773.1:p.Ile338=
ENST00000642627.1:c.1013_1020delinsTAACTGAA	ENSP00000496772.1:p.Ile338=
ENST00000642646.1:c.1013_1020delinsTAACTGAA	ENSP00000496292.1:p.Ile338=
ENST00000642745.1:c.1013_1020delinsTAACTGAA	ENSP00000493963.1:p.Ile338=
ENST00000642811.1:c.*783_*790delinsTAACTGAA	ENSP00000495554.1:n.*783_*790delinsTAACTG...
ENST00000642854.1:c.*798_*805delinsTAACTGAA	ENSP00000494639.1:n.*798_*805delinsTAACTG...
ENST00000643072.1:c.860_867delinsTAACTGAA	ENSP00000496691.1:p.Ile287=
ENST00000643362.1:c.860_867delinsTAACTGAA	ENSP00000496398.1:p.Ile287=
ENST00000643583.1:c.1013_1020delinsTAACTGAA	ENSP00000494685.1:p.Ile338=
ENST00000643875.1:c.1013_1020delinsTAACTGAA	ENSP00000495158.1:p.Ile338=
ENST00000644097.1:c.1013_1020delinsTAACTGAA	ENSP00000494682.1:p.Ile338=
ENST00000644255.1:c.*783_*790delinsTAACTGAA	ENSP00000493608.1:n.*783_*790delinsTAACTG...
ENST00000644319.1:n.740_747delinsTAACTGAA
ENST00000644997.1:c.*670_*677delinsTAACTGAA	ENSP00000495654.1:n.*670_*677delinsTAACTG...
ENST00000645129.1:c.860_867delinsTAACTGAA	ENSP00000493639.1:p.Ile287=
ENST00000645150.1:c.1013_1020delinsTAACTGAA	ENSP00000494365.1:p.Ile338=
ENST00000645901.1:n.1216_1223delinsTAACTGAA
ENST00000646391.1:c.*783_*790delinsTAACTGAA	ENSP00000494104.1:n.*783_*790delinsTAACTG...
ENST00000646625.1:c.1013_1020delinsTAACTGAA	ENSP00000496263.1:p.Ile338=
ENST00000647078.1:c.1013_1020delinsTAACTGAA	ENSP00000496066.1:p.Ile338=
ENST00000647279.1:c.*252_*259delinsTAACTGAA	ENSP00000494502.1:n.*252_*259delinsTAACTG...
ENST00000647462.1:c.1013_1020delinsTAACTGAA	ENSP00000495821.1:p.Ile338=
ENST00000647506.1:n.1241_1248delinsTAACTGAA
ENST00000298552.7:c.1013_1020delinsTAACTGAA	ENSP00000298552.3:p.Ile338=
ENST00000403810.5:c.1013_1020delinsTAACTGAA	ENSP00000386093.1:p.Ile338=
ENST00000440111.6:c.1013_1020delinsTAACTGAA	ENSP00000394524.2:p.Ile338=
ENST00000493467.5:n.1209_1216delinsTAACTGAA
ENST00000545250.5:c.860_867delinsTAACTGAA	ENSP00000444017.1:p.Ile287=
NM_000368.4:c.1013_1020delinsTAACTGAA , LRG_486t1:c.1013_1020delinsTAACTGAA	NP_000359.1:p.Ile338=
NM_001162426.1:c.1013_1020delinsTAACTGAA	NP_001155898.1:p.Ile338=
NM_001162427.1:c.860_867delinsTAACTGAA	NP_001155899.1:p.Ile287=
XM_005272211.1:c.1013_1020delinsTAACTGAA	XP_005272268.1:p.Ile338=
XM_006717271.1:c.1013_1020delinsTAACTGAA	XP_006717334.1:p.Ile338=
XM_006717272.2:c.1013_1020delinsTAACTGAA	XP_006717335.1:p.Ile338=
XM_011518979.1:c.1013_1020delinsTAACTGAA	XP_011517281.1:p.Ile338=
NM_001362177.1:c.650_657delinsTAACTGAA	NP_001349106.1:p.Ile217=
XM_011518979.2:c.1013_1020delinsTAACTGAA	XP_011517281.1:p.Ile338=
XM_017015096.1:c.1013_1020delinsTAACTGAA	XP_016870585.1:p.Ile338=
XM_017015097.1:c.1013_1020delinsTAACTGAA	XP_016870586.1:p.Ile338=
XM_017015098.1:c.1013_1020delinsTAACTGAA	XP_016870587.1:p.Ile338=
XM_017015100.1:c.650_657delinsTAACTGAA	XP_016870589.1:p.Ile217=
XM_017015101.1:c.650_657delinsTAACTGAA	XP_016870590.1:p.Ile217=
NM_000368.5:c.1013_1020delinsTAACTGAA MANE Select	NP_000359.1:p.Ile338=
NM_001162426.2:c.1013_1020delinsTAACTGAA	NP_001155898.1:p.Ile338=
NM_001162427.2:c.860_867delinsTAACTGAA	NP_001155899.1:p.Ile287=
NM_001362177.2:c.650_657delinsTAACTGAA	NP_001349106.1:p.Ile217=