Canonical Allele Identifier: CA1882409597

Gene: TSC1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132902775T= , CM000671.2:g.132902775T=	GRCh38
NC_000009.11:g.135778162T= , CM000671.1:g.135778162T=	GRCh37
NC_000009.10:g.134767983T=	NCBI36
NG_012386.1:g.46859A= , LRG_486:g.46859A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475903.7:c.2218A=	ENSP00000496126.2:p.Lys740=
ENST00000490179.4:c.2221A=	ENSP00000495533.2:p.Lys741=
ENST00000642261.2:c.2217A=	ENSP00000494743.2:p.Ter739=
ENST00000643275.2:c.*161A=	ENSP00000495598.2:n.*161A=
ENST00000643362.2:c.1834A=	ENSP00000496398.2:p.Lys612=
ENST00000643625.2:c.2054A=	ENSP00000495546.2:p.Glu685=
ENST00000643691.2:c.1858A=	ENSP00000494916.2:p.Lys620=
ENST00000644184.2:c.2221A=	ENSP00000495428.2:p.Lys741=
ENST00000645129.2:c.2065A=	ENSP00000493639.2:p.Lys689=
ENST00000646440.2:c.2221A=	ENSP00000495830.2:p.Lys741=
ENST00000298552.9:c.2221A= MANE Select	ENSP00000298552.3:p.Lys741=
ENST00000642261.1:c.281A=
ENST00000642617.1:c.2218A=	ENSP00000493773.1:p.Lys740=
ENST00000642627.1:c.2203A=	ENSP00000496772.1:p.Lys735=
ENST00000642811.1:c.*1991A=	ENSP00000495554.1:n.*1991A=
ENST00000643072.1:c.2068A=	ENSP00000496691.1:p.Lys690=
ENST00000643275.1:c.695A=	ENSP00000495598.1:n.695A=
ENST00000643583.1:c.2206A=	ENSP00000494685.1:p.Lys736=
ENST00000643625.1:c.98A=	ENSP00000495546.1:p.Glu33=
ENST00000643875.1:c.2221A=	ENSP00000495158.1:p.Lys741=
ENST00000644097.1:c.2218A=	ENSP00000494682.1:p.Lys740=
ENST00000644184.1:c.958A=	ENSP00000495428.1:p.Lys320=
ENST00000644255.1:c.*1988A=	ENSP00000493608.1:n.*1988A=
ENST00000644319.1:n.2596A=
ENST00000644882.1:n.1176A=
ENST00000645901.1:n.3072A=
ENST00000646391.1:c.*1991A=	ENSP00000494104.1:n.*1991A=
ENST00000646625.1:c.2221A=	ENSP00000496263.1:p.Lys741=
ENST00000647262.1:n.1186A=
ENST00000647279.1:c.*1460A=	ENSP00000494502.1:n.*1460A=
ENST00000647506.1:n.3097A=
ENST00000647534.1:n.1285A=
ENST00000298552.7:c.2221A=	ENSP00000298552.3:p.Lys741=
ENST00000440111.6:c.2221A=	ENSP00000394524.2:p.Lys741=
ENST00000545250.5:c.2068A=	ENSP00000444017.1:p.Lys690=
NM_000368.4:c.2221A= , LRG_486t1:c.2221A=	NP_000359.1:p.Lys741=
NM_001162426.1:c.2218A=	NP_001155898.1:p.Lys740=
NM_001162427.1:c.2068A=	NP_001155899.1:p.Lys690=
XM_005272211.1:c.2221A=	XP_005272268.1:p.Lys741=
XM_006717271.1:c.2221A=	XP_006717334.1:p.Lys741=
XM_011518979.1:c.2221A=	XP_011517281.1:p.Lys741=
NM_001362177.1:c.1858A=	NP_001349106.1:p.Lys620=
XM_011518979.2:c.2221A=	XP_011517281.1:p.Lys741=
XM_017015096.1:c.2221A=	XP_016870585.1:p.Lys741=
XM_017015097.1:c.2221A=	XP_016870586.1:p.Lys741=
XM_017015098.1:c.2218A=	XP_016870587.1:p.Lys740=
XM_017015100.1:c.1858A=	XP_016870589.1:p.Lys620=
XM_017015101.1:c.1855A=	XP_016870590.1:p.Lys619=
NM_000368.5:c.2221A= MANE Select	NP_000359.1:p.Lys741=
NM_001162426.2:c.2218A=	NP_001155898.1:p.Lys740=
NM_001162427.2:c.2068A=	NP_001155899.1:p.Lys690=
NM_001362177.2:c.1858A=	NP_001349106.1:p.Lys620=