Canonical Allele Identifier: CA1882406086
Gene: TSC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.132900793G= , CM000671.2:g.132900793G= GRCh38
NC_000009.11:g.135776180G= , CM000671.1:g.135776180G= GRCh37
NC_000009.10:g.134766001G= NCBI36
NG_012386.1:g.48841C= , LRG_486:g.48841C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000475903.7:c.2544C= ENSP00000496126.2:p.Asn848=
ENST00000490179.4:c.2547C= ENSP00000495533.2:p.Asn849=
ENST00000642261.2:c.*326C= ENSP00000494743.2:n.*326C=
ENST00000643275.2:c.*487C= ENSP00000495598.2:n.*487C=
ENST00000643362.2:c.2160C= ENSP00000496398.2:p.Asn720=
ENST00000643625.2:c.*289C= ENSP00000495546.2:n.*289C=
ENST00000643691.2:c.2184C= ENSP00000494916.2:p.Asn728=
ENST00000644184.2:c.2505C= ENSP00000495428.2:p.Asn835=
ENST00000645129.2:c.2391C= ENSP00000493639.2:p.Asn797=
ENST00000646440.2:c.2547C= ENSP00000495830.2:p.Asn849=
ENST00000298552.9:c.2547C= MANE Select ENSP00000298552.3:p.Asn849=
ENST00000642261.1:c.607C=
ENST00000642617.1:c.2544C= ENSP00000493773.1:p.Asn848=
ENST00000642627.1:c.2529C= ENSP00000496772.1:p.Asn843=
ENST00000642811.1:c.*2317C= ENSP00000495554.1:n.*2317C=
ENST00000643072.1:c.2394C= ENSP00000496691.1:p.Asn798=
ENST00000643275.1:c.1021C= ENSP00000495598.1:n.1021C=
ENST00000643583.1:c.2532C= ENSP00000494685.1:p.Asn844=
ENST00000643625.1:c.424C= ENSP00000495546.1:n.424C=
ENST00000643875.1:c.2547C= ENSP00000495158.1:p.Asn849=
ENST00000644097.1:c.2544C= ENSP00000494682.1:p.Asn848=
ENST00000644184.1:c.1242C= ENSP00000495428.1:p.Asn414=
ENST00000644255.1:c.*2314C= ENSP00000493608.1:n.*2314C=
ENST00000644319.1:n.2922C=
ENST00000644786.1:n.206C=
ENST00000644882.1:n.1460C=
ENST00000645901.1:n.3398C=
ENST00000646391.1:c.*2317C= ENSP00000494104.1:n.*2317C=
ENST00000646625.1:c.2547C= ENSP00000496263.1:p.Asn849=
ENST00000647262.1:n.1512C=
ENST00000647279.1:c.*1786C= ENSP00000494502.1:n.*1786C=
ENST00000647506.1:n.3423C=
ENST00000647534.1:n.1611C=
ENST00000298552.7:c.2547C= ENSP00000298552.3:p.Asn849=
ENST00000440111.6:c.2547C= ENSP00000394524.2:p.Asn849=
ENST00000545250.5:c.2394C= ENSP00000444017.1:p.Asn798=
NM_000368.4:c.2547C= , LRG_486t1:c.2547C= NP_000359.1:p.Asn849=
NM_001162426.1:c.2544C= NP_001155898.1:p.Asn848=
NM_001162427.1:c.2394C= NP_001155899.1:p.Asn798=
XM_005272211.1:c.2547C= XP_005272268.1:p.Asn849=
XM_006717271.1:c.2547C= XP_006717334.1:p.Asn849=
XM_011518979.1:c.2547C= XP_011517281.1:p.Asn849=
NM_001362177.1:c.2184C= NP_001349106.1:p.Asn728=
XM_011518979.2:c.2547C= XP_011517281.1:p.Asn849=
XM_017015096.1:c.2547C= XP_016870585.1:p.Asn849=
XM_017015097.1:c.2547C= XP_016870586.1:p.Asn849=
XM_017015098.1:c.2544C= XP_016870587.1:p.Asn848=
XM_017015100.1:c.2184C= XP_016870589.1:p.Asn728=
XM_017015101.1:c.2181C= XP_016870590.1:p.Asn727=
NM_000368.5:c.2547C= MANE Select NP_000359.1:p.Asn849=
NM_001162426.2:c.2544C= NP_001155898.1:p.Asn848=
NM_001162427.2:c.2394C= NP_001155899.1:p.Asn798=
NM_001362177.2:c.2184C= NP_001349106.1:p.Asn728=