Canonical Allele Identifier: CA375367339

Gene: TSC1

Linked Data

• MyVariant Identifiers: chr9:g.135771996T>G (hg19) ; chr9:g.132896609T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132896609T>G , CM000671.2:g.132896609T>G	GRCh38
NC_000009.11:g.135771996T>G , CM000671.1:g.135771996T>G	GRCh37
NC_000009.10:g.134761817T>G	NCBI36
NG_012386.1:g.53025A>C , LRG_486:g.53025A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475903.7:c.3118A>C	ENSP00000496126.2:p.Ser1040Arg
ENST00000490179.4:c.3121A>C	ENSP00000495533.2:p.Ser1041Arg
ENST00000642261.2:c.*977A>C	ENSP00000494743.2:n.*977A>C
ENST00000643275.2:c.*1061A>C	ENSP00000495598.2:n.*1061A>C
ENST00000643362.2:c.2734A>C	ENSP00000496398.2:p.Ser912Arg
ENST00000643625.2:c.*863A>C	ENSP00000495546.2:n.*863A>C
ENST00000643691.2:c.2758A>C	ENSP00000494916.2:p.Ser920Arg
ENST00000644184.2:c.3079A>C	ENSP00000495428.2:p.Ser1027Arg
ENST00000645129.2:c.2965A>C	ENSP00000493639.2:p.Ser989Arg
ENST00000646440.2:c.3121A>C	ENSP00000495830.2:p.Ser1041Arg
ENST00000298552.9:c.3121A>C MANE Select	ENSP00000298552.3:p.Ser1041Arg
ENST00000642261.1:c.1258A>C
ENST00000642617.1:c.3118A>C	ENSP00000493773.1:p.Ser1040Arg
ENST00000642627.1:c.3103A>C	ENSP00000496772.1:p.Ser1035Arg
ENST00000642811.1:c.*2891A>C	ENSP00000495554.1:n.*2891A>C
ENST00000643072.1:c.2968A>C	ENSP00000496691.1:p.Ser990Arg
ENST00000643275.1:c.1595A>C	ENSP00000495598.1:n.1595A>C
ENST00000643583.1:c.3106A>C	ENSP00000494685.1:p.Ser1036Arg
ENST00000643625.1:c.998A>C	ENSP00000495546.1:n.998A>C
ENST00000643875.1:c.3121A>C	ENSP00000495158.1:p.Ser1041Arg
ENST00000644097.1:c.3118A>C	ENSP00000494682.1:p.Ser1040Arg
ENST00000644184.1:c.1816A>C	ENSP00000495428.1:p.Ser606Arg
ENST00000644255.1:c.*2888A>C	ENSP00000493608.1:n.*2888A>C
ENST00000644319.1:n.3496A>C
ENST00000644786.1:n.780A>C
ENST00000644882.1:n.2029A>C
ENST00000645901.1:n.3972A>C
ENST00000646391.1:c.*2891A>C	ENSP00000494104.1:n.*2891A>C
ENST00000646625.1:c.3121A>C	ENSP00000496263.1:p.Ser1041Arg
ENST00000647262.1:n.2086A>C
ENST00000647279.1:c.*2360A>C	ENSP00000494502.1:n.*2360A>C
ENST00000647534.1:n.2185A>C
ENST00000298552.7:c.3121A>C	ENSP00000298552.3:p.Ser1041Arg
ENST00000440111.6:c.3121A>C	ENSP00000394524.2:p.Ser1041Arg
ENST00000545250.5:c.2968A>C	ENSP00000444017.1:p.Ser990Arg
NM_000368.4:c.3121A>C , LRG_486t1:c.3121A>C	NP_000359.1:p.Ser1041Arg
NM_001162426.1:c.3118A>C	NP_001155898.1:p.Ser1040Arg
NM_001162427.1:c.2968A>C	NP_001155899.1:p.Ser990Arg
XM_005272211.1:c.3121A>C	XP_005272268.1:p.Ser1041Arg
XM_006717271.1:c.3121A>C	XP_006717334.1:p.Ser1041Arg
XM_011518979.1:c.3121A>C	XP_011517281.1:p.Ser1041Arg
NM_001362177.1:c.2758A>C	NP_001349106.1:p.Ser920Arg
XM_011518979.2:c.3121A>C	XP_011517281.1:p.Ser1041Arg
XM_017015096.1:c.3121A>C	XP_016870585.1:p.Ser1041Arg
XM_017015097.1:c.3121A>C	XP_016870586.1:p.Ser1041Arg
XM_017015098.1:c.3118A>C	XP_016870587.1:p.Ser1040Arg
XM_017015100.1:c.2758A>C	XP_016870589.1:p.Ser920Arg
XM_017015101.1:c.2755A>C	XP_016870590.1:p.Ser919Arg
NM_000368.5:c.3121A>C MANE Select	NP_000359.1:p.Ser1041Arg
NM_001162426.2:c.3118A>C	NP_001155898.1:p.Ser1040Arg
NM_001162427.2:c.2968A>C	NP_001155899.1:p.Ser990Arg
NM_001362177.2:c.2758A>C	NP_001349106.1:p.Ser920Arg