Canonical Allele Identifier: CA10578830

Gene: TSC1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132911085C>T , CM000671.2:g.132911085C>T	GRCh38
NC_000009.11:g.135786472C>T , CM000671.1:g.135786472C>T	GRCh37
NC_000009.10:g.134776293C>T	NCBI36
NG_012386.1:g.38549G>A , LRG_486:g.38549G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000368.5:c.1058G>A MANE Select	NP_000359.1:p.Cys353Tyr
ENST00000298552.9:c.1058G>A MANE Select	ENSP00000298552.3:p.Cys353Tyr
NM_000368.4:c.1058G>A , LRG_486t1:c.1058G>A	NP_000359.1:p.Cys353Tyr
NM_001162426.1:c.1058G>A	NP_001155898.1:p.Cys353Tyr
NM_001162426.2:c.1058G>A	NP_001155898.1:p.Cys353Tyr
NM_001162427.1:c.905G>A	NP_001155899.1:p.Cys302Tyr
NM_001162427.2:c.905G>A	NP_001155899.1:p.Cys302Tyr
NM_001362177.1:c.695G>A	NP_001349106.1:p.Cys232Tyr
NM_001362177.2:c.695G>A	NP_001349106.1:p.Cys232Tyr
ENST00000298552.7:c.1058G>A	ENSP00000298552.3:p.Cys353Tyr
ENST00000403810.6:c.*296G>A	ENSP00000386093.1:n.*296G>A
ENST00000440111.6:c.1058G>A	ENSP00000394524.2:p.Cys353Tyr
ENST00000475903.7:c.1058G>A	ENSP00000496126.2:p.Cys353Tyr
ENST00000490179.4:c.1058G>A	ENSP00000495533.2:p.Cys353Tyr
ENST00000493467.5:n.1254G>A
ENST00000493467.6:n.332G>A
ENST00000545250.5:c.905G>A	ENSP00000444017.1:p.Cys302Tyr
ENST00000642261.2:c.1058G>A	ENSP00000494743.2:p.Cys353Tyr
ENST00000642344.1:c.*799G>A	ENSP00000494847.1:n.*799G>A
ENST00000642617.1:c.1058G>A	ENSP00000493773.1:p.Cys353Tyr
ENST00000642627.1:c.1058G>A	ENSP00000496772.1:p.Cys353Tyr
ENST00000642646.1:c.1058G>A	ENSP00000496292.1:p.Cys353Tyr
ENST00000642745.1:c.1058G>A	ENSP00000493963.1:p.Cys353Tyr
ENST00000642811.1:c.*828G>A	ENSP00000495554.1:n.*828G>A
ENST00000643072.1:c.905G>A	ENSP00000496691.1:p.Cys302Tyr
ENST00000643275.2:c.1058G>A	ENSP00000495598.2:p.Cys353Tyr
ENST00000643362.1:c.876+368G>A	ENSP00000496398.1:n.876+368G>A
ENST00000643362.2:c.876+368G>A	ENSP00000496398.2:n.876+368G>A
ENST00000643583.1:c.1058G>A	ENSP00000494685.1:p.Cys353Tyr
ENST00000643625.2:c.1058G>A	ENSP00000495546.2:p.Cys353Tyr
ENST00000643691.2:c.695G>A	ENSP00000494916.2:p.Cys232Tyr
ENST00000643875.1:c.1058G>A	ENSP00000495158.1:p.Cys353Tyr
ENST00000644097.1:c.1058G>A	ENSP00000494682.1:p.Cys353Tyr
ENST00000644184.2:c.1058G>A	ENSP00000495428.2:p.Cys353Tyr
ENST00000644255.1:c.*828G>A	ENSP00000493608.1:n.*828G>A
ENST00000644319.1:n.1124G>A
ENST00000644997.1:c.*715G>A	ENSP00000495654.1:n.*715G>A
ENST00000645129.1:c.905G>A	ENSP00000493639.1:p.Cys302Tyr
ENST00000645129.2:c.905G>A	ENSP00000493639.2:p.Cys302Tyr
ENST00000645150.1:c.1058G>A	ENSP00000494365.1:p.Cys353Tyr
ENST00000645901.1:n.1600G>A
ENST00000646391.1:c.*828G>A	ENSP00000494104.1:n.*828G>A
ENST00000646440.2:c.1058G>A	ENSP00000495830.2:p.Cys353Tyr
ENST00000646625.1:c.1058G>A	ENSP00000496263.1:p.Cys353Tyr
ENST00000647078.1:c.1101G>A	ENSP00000496066.1:p.Leu367=
ENST00000647078.2:c.1101G>A	ENSP00000496066.1:p.Leu367=
ENST00000647279.1:c.*297G>A	ENSP00000494502.1:n.*297G>A
ENST00000647462.1:c.1058G>A	ENSP00000495821.1:p.Cys353Tyr
ENST00000647506.1:n.1625G>A
ENST00000647534.1:n.122G>A
XM_005272211.1:c.1058G>A	XP_005272268.1:p.Cys353Tyr
XM_006717271.1:c.1058G>A	XP_006717334.1:p.Cys353Tyr
XM_006717272.2:c.1058G>A	XP_006717335.1:p.Cys353Tyr
XM_011518979.1:c.1058G>A	XP_011517281.1:p.Cys353Tyr
XM_011518979.2:c.1058G>A	XP_011517281.1:p.Cys353Tyr
XM_017015096.1:c.1058G>A	XP_016870585.1:p.Cys353Tyr
XM_017015097.1:c.1058G>A	XP_016870586.1:p.Cys353Tyr
XM_017015098.1:c.1058G>A	XP_016870587.1:p.Cys353Tyr
XM_017015100.1:c.695G>A	XP_016870589.1:p.Cys232Tyr
XM_017015101.1:c.695G>A	XP_016870590.1:p.Cys232Tyr