Canonical Allele Identifier: CA1882415645

Gene: TSC1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132907348C= , CM000671.2:g.132907348C=	GRCh38
NC_000009.11:g.135782735C= , CM000671.1:g.135782735C=	GRCh37
NC_000009.10:g.134772556C=	NCBI36
NG_012386.1:g.42286G= , LRG_486:g.42286G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475903.7:c.1283G=	ENSP00000496126.2:p.Arg428=
ENST00000490179.4:c.1286G=	ENSP00000495533.2:p.Arg429=
ENST00000642261.2:c.1286G=	ENSP00000494743.2:p.Arg429=
ENST00000643275.2:c.1286G=	ENSP00000495598.2:p.Arg429=
ENST00000643362.2:c.899G=	ENSP00000496398.2:p.Arg300=
ENST00000643625.2:c.1286G=	ENSP00000495546.2:p.Arg429=
ENST00000643691.2:c.923G=	ENSP00000494916.2:p.Arg308=
ENST00000644184.2:c.1286G=	ENSP00000495428.2:p.Arg429=
ENST00000645129.2:c.1130G=	ENSP00000493639.2:p.Arg377=
ENST00000646440.2:c.1286G=	ENSP00000495830.2:p.Arg429=
ENST00000298552.9:c.1286G= MANE Select	ENSP00000298552.3:p.Arg429=
ENST00000642344.1:c.*1027G=	ENSP00000494847.1:n.*1027G=
ENST00000642617.1:c.1283G=	ENSP00000493773.1:p.Arg428=
ENST00000642627.1:c.1283G=	ENSP00000496772.1:p.Arg428=
ENST00000642811.1:c.*1056G=	ENSP00000495554.1:n.*1056G=
ENST00000643072.1:c.1133G=	ENSP00000496691.1:p.Arg378=
ENST00000643362.1:c.899G=	ENSP00000496398.1:p.Arg300=
ENST00000643583.1:c.1286G=	ENSP00000494685.1:p.Arg429=
ENST00000643875.1:c.1286G=	ENSP00000495158.1:p.Arg429=
ENST00000644097.1:c.1283G=	ENSP00000494682.1:p.Arg428=
ENST00000644184.1:c.23G=	ENSP00000495428.1:p.Arg8=
ENST00000644255.1:c.*1053G=	ENSP00000493608.1:n.*1053G=
ENST00000644319.1:n.1661G=
ENST00000645901.1:n.2137G=
ENST00000646391.1:c.*1056G=	ENSP00000494104.1:n.*1056G=
ENST00000646625.1:c.1286G=	ENSP00000496263.1:p.Arg429=
ENST00000647279.1:c.*525G=	ENSP00000494502.1:n.*525G=
ENST00000647506.1:n.2162G=
ENST00000647534.1:n.350G=
ENST00000298552.7:c.1286G=	ENSP00000298552.3:p.Arg429=
ENST00000440111.6:c.1286G=	ENSP00000394524.2:p.Arg429=
ENST00000545250.5:c.1133G=	ENSP00000444017.1:p.Arg378=
NM_000368.4:c.1286G= , LRG_486t1:c.1286G=	NP_000359.1:p.Arg429=
NM_001162426.1:c.1283G=	NP_001155898.1:p.Arg428=
NM_001162427.1:c.1133G=	NP_001155899.1:p.Arg378=
XM_005272211.1:c.1286G=	XP_005272268.1:p.Arg429=
XM_006717271.1:c.1286G=	XP_006717334.1:p.Arg429=
XM_006717272.2:c.1286G=	XP_006717335.1:p.Arg429=
XM_011518979.1:c.1286G=	XP_011517281.1:p.Arg429=
NM_001362177.1:c.923G=	NP_001349106.1:p.Arg308=
XM_011518979.2:c.1286G=	XP_011517281.1:p.Arg429=
XM_017015096.1:c.1286G=	XP_016870585.1:p.Arg429=
XM_017015097.1:c.1286G=	XP_016870586.1:p.Arg429=
XM_017015098.1:c.1283G=	XP_016870587.1:p.Arg428=
XM_017015100.1:c.923G=	XP_016870589.1:p.Arg308=
XM_017015101.1:c.920G=	XP_016870590.1:p.Arg307=
NM_000368.5:c.1286G= MANE Select	NP_000359.1:p.Arg429=
NM_001162426.2:c.1283G=	NP_001155898.1:p.Arg428=
NM_001162427.2:c.1133G=	NP_001155899.1:p.Arg378=
NM_001362177.2:c.923G=	NP_001349106.1:p.Arg308=