Canonical Allele Identifier: CA1882410770

Gene: TSC1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132903686T= , CM000671.2:g.132903686T=	GRCh38
NC_000009.11:g.135779073T= , CM000671.1:g.135779073T=	GRCh37
NC_000009.10:g.134768894T=	NCBI36
NG_012386.1:g.45948A= , LRG_486:g.45948A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475903.7:c.2170A=	ENSP00000496126.2:p.Lys724=
ENST00000490179.4:c.2173A=	ENSP00000495533.2:p.Lys725=
ENST00000642261.2:c.2173A=	ENSP00000494743.2:p.Lys725=
ENST00000643275.2:c.*113A=	ENSP00000495598.2:n.*113A=
ENST00000643362.2:c.1786A=	ENSP00000496398.2:p.Lys596=
ENST00000643625.2:c.2041+725A=	ENSP00000495546.2:n.2041+725A=
ENST00000643691.2:c.1810A=	ENSP00000494916.2:p.Lys604=
ENST00000644184.2:c.2173A=	ENSP00000495428.2:p.Lys725=
ENST00000645129.2:c.2017A=	ENSP00000493639.2:p.Lys673=
ENST00000646440.2:c.2173A=	ENSP00000495830.2:p.Lys725=
ENST00000298552.9:c.2173A= MANE Select	ENSP00000298552.3:p.Lys725=
ENST00000642261.1:c.237A=
ENST00000642617.1:c.2170A=	ENSP00000493773.1:p.Lys724=
ENST00000642627.1:c.2155A=	ENSP00000496772.1:p.Lys719=
ENST00000642811.1:c.*1943A=	ENSP00000495554.1:n.*1943A=
ENST00000643072.1:c.2020A=	ENSP00000496691.1:p.Lys674=
ENST00000643275.1:c.647A=	ENSP00000495598.1:n.647A=
ENST00000643583.1:c.2158A=	ENSP00000494685.1:p.Lys720=
ENST00000643625.1:c.85+725A=	ENSP00000495546.1:n.85+725A=
ENST00000643875.1:c.2173A=	ENSP00000495158.1:p.Lys725=
ENST00000644097.1:c.2170A=	ENSP00000494682.1:p.Lys724=
ENST00000644184.1:c.910A=	ENSP00000495428.1:p.Lys304=
ENST00000644255.1:c.*1940A=	ENSP00000493608.1:n.*1940A=
ENST00000644319.1:n.2548A=
ENST00000644882.1:n.1128A=
ENST00000645901.1:n.3024A=
ENST00000646391.1:c.*1943A=	ENSP00000494104.1:n.*1943A=
ENST00000646625.1:c.2173A=	ENSP00000496263.1:p.Lys725=
ENST00000647262.1:n.1138A=
ENST00000647279.1:c.*1412A=	ENSP00000494502.1:n.*1412A=
ENST00000647506.1:n.3049A=
ENST00000647534.1:n.1237A=
ENST00000298552.7:c.2173A=	ENSP00000298552.3:p.Lys725=
ENST00000440111.6:c.2173A=	ENSP00000394524.2:p.Lys725=
ENST00000545250.5:c.2020A=	ENSP00000444017.1:p.Lys674=
NM_000368.4:c.2173A= , LRG_486t1:c.2173A=	NP_000359.1:p.Lys725=
NM_001162426.1:c.2170A=	NP_001155898.1:p.Lys724=
NM_001162427.1:c.2020A=	NP_001155899.1:p.Lys674=
XM_005272211.1:c.2173A=	XP_005272268.1:p.Lys725=
XM_006717271.1:c.2173A=	XP_006717334.1:p.Lys725=
XM_011518979.1:c.2173A=	XP_011517281.1:p.Lys725=
NM_001362177.1:c.1810A=	NP_001349106.1:p.Lys604=
XM_011518979.2:c.2173A=	XP_011517281.1:p.Lys725=
XM_017015096.1:c.2173A=	XP_016870585.1:p.Lys725=
XM_017015097.1:c.2173A=	XP_016870586.1:p.Lys725=
XM_017015098.1:c.2170A=	XP_016870587.1:p.Lys724=
XM_017015100.1:c.1810A=	XP_016870589.1:p.Lys604=
XM_017015101.1:c.1807A=	XP_016870590.1:p.Lys603=
NM_000368.5:c.2173A= MANE Select	NP_000359.1:p.Lys725=
NM_001162426.2:c.2170A=	NP_001155898.1:p.Lys724=
NM_001162427.2:c.2020A=	NP_001155899.1:p.Lys674=
NM_001362177.2:c.1810A=	NP_001349106.1:p.Lys604=