Canonical Allele Identifier: CA467590665

Gene: TSC1

Linked Data

• MyVariant Identifiers: chr9:g.135779062A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132903675A>G , CM000671.2:g.132903675A>G	GRCh38
NC_000009.11:g.135779062A>G , CM000671.1:g.135779062A>G	GRCh37
NC_000009.10:g.134768883A>G	NCBI36
NG_012386.1:g.45959T>C , LRG_486:g.45959T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475903.7:c.2181T>C	ENSP00000496126.2:p.Ala727=
ENST00000490179.4:c.2184T>C	ENSP00000495533.2:p.Ala728=
ENST00000642261.2:c.2184T>C	ENSP00000494743.2:p.Ala728=
ENST00000643275.2:c.*124T>C	ENSP00000495598.2:n.*124T>C
ENST00000643362.2:c.1797T>C	ENSP00000496398.2:p.Ala599=
ENST00000643625.2:c.2041+736T>C	ENSP00000495546.2:n.2041+736T>C
ENST00000643691.2:c.1821T>C	ENSP00000494916.2:p.Ala607=
ENST00000644184.2:c.2184T>C	ENSP00000495428.2:p.Ala728=
ENST00000645129.2:c.2028T>C	ENSP00000493639.2:p.Ala676=
ENST00000646440.2:c.2184T>C	ENSP00000495830.2:p.Ala728=
ENST00000298552.9:c.2184T>C MANE Select	ENSP00000298552.3:p.Ala728=
ENST00000642261.1:c.248T>C
ENST00000642617.1:c.2181T>C	ENSP00000493773.1:p.Ala727=
ENST00000642627.1:c.2166T>C	ENSP00000496772.1:p.Ala722=
ENST00000642811.1:c.*1954T>C	ENSP00000495554.1:n.*1954T>C
ENST00000643072.1:c.2031T>C	ENSP00000496691.1:p.Ala677=
ENST00000643275.1:c.658T>C	ENSP00000495598.1:n.658T>C
ENST00000643583.1:c.2169T>C	ENSP00000494685.1:p.Ala723=
ENST00000643625.1:c.85+736T>C	ENSP00000495546.1:n.85+736T>C
ENST00000643875.1:c.2184T>C	ENSP00000495158.1:p.Ala728=
ENST00000644097.1:c.2181T>C	ENSP00000494682.1:p.Ala727=
ENST00000644184.1:c.921T>C	ENSP00000495428.1:p.Ala307=
ENST00000644255.1:c.*1951T>C	ENSP00000493608.1:n.*1951T>C
ENST00000644319.1:n.2559T>C
ENST00000644882.1:n.1139T>C
ENST00000645901.1:n.3035T>C
ENST00000646391.1:c.*1954T>C	ENSP00000494104.1:n.*1954T>C
ENST00000646625.1:c.2184T>C	ENSP00000496263.1:p.Ala728=
ENST00000647262.1:n.1149T>C
ENST00000647279.1:c.*1423T>C	ENSP00000494502.1:n.*1423T>C
ENST00000647506.1:n.3060T>C
ENST00000647534.1:n.1248T>C
ENST00000298552.7:c.2184T>C	ENSP00000298552.3:p.Ala728=
ENST00000440111.6:c.2184T>C	ENSP00000394524.2:p.Ala728=
ENST00000545250.5:c.2031T>C	ENSP00000444017.1:p.Ala677=
NM_000368.4:c.2184T>C , LRG_486t1:c.2184T>C	NP_000359.1:p.Ala728=
NM_001162426.1:c.2181T>C	NP_001155898.1:p.Ala727=
NM_001162427.1:c.2031T>C	NP_001155899.1:p.Ala677=
XM_005272211.1:c.2184T>C	XP_005272268.1:p.Ala728=
XM_006717271.1:c.2184T>C	XP_006717334.1:p.Ala728=
XM_011518979.1:c.2184T>C	XP_011517281.1:p.Ala728=
NM_001362177.1:c.1821T>C	NP_001349106.1:p.Ala607=
XM_011518979.2:c.2184T>C	XP_011517281.1:p.Ala728=
XM_017015096.1:c.2184T>C	XP_016870585.1:p.Ala728=
XM_017015097.1:c.2184T>C	XP_016870586.1:p.Ala728=
XM_017015098.1:c.2181T>C	XP_016870587.1:p.Ala727=
XM_017015100.1:c.1821T>C	XP_016870589.1:p.Ala607=
XM_017015101.1:c.1818T>C	XP_016870590.1:p.Ala606=
NM_000368.5:c.2184T>C MANE Select	NP_000359.1:p.Ala728=
NM_001162426.2:c.2181T>C	NP_001155898.1:p.Ala727=
NM_001162427.2:c.2031T>C	NP_001155899.1:p.Ala677=
NM_001362177.2:c.1821T>C	NP_001349106.1:p.Ala607=