Canonical Allele Identifier: CA1882405906
Gene: TSC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.132900750C= , CM000671.2:g.132900750C= GRCh38
NC_000009.11:g.135776137C= , CM000671.1:g.135776137C= GRCh37
NC_000009.10:g.134765958C= NCBI36
NG_012386.1:g.48884G= , LRG_486:g.48884G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000475903.7:c.2587G= ENSP00000496126.2:p.Glu863=
ENST00000490179.4:c.2590G= ENSP00000495533.2:p.Glu864=
ENST00000642261.2:c.*369G= ENSP00000494743.2:n.*369G=
ENST00000643275.2:c.*530G= ENSP00000495598.2:n.*530G=
ENST00000643362.2:c.2203G= ENSP00000496398.2:p.Glu735=
ENST00000643625.2:c.*332G= ENSP00000495546.2:n.*332G=
ENST00000643691.2:c.2227G= ENSP00000494916.2:p.Glu743=
ENST00000644184.2:c.2548G= ENSP00000495428.2:p.Glu850=
ENST00000645129.2:c.2434G= ENSP00000493639.2:p.Glu812=
ENST00000646440.2:c.2590G= ENSP00000495830.2:p.Glu864=
ENST00000298552.9:c.2590G= MANE Select ENSP00000298552.3:p.Glu864=
ENST00000642261.1:c.650G=
ENST00000642617.1:c.2587G= ENSP00000493773.1:p.Glu863=
ENST00000642627.1:c.2572G= ENSP00000496772.1:p.Glu858=
ENST00000642811.1:c.*2360G= ENSP00000495554.1:n.*2360G=
ENST00000643072.1:c.2437G= ENSP00000496691.1:p.Glu813=
ENST00000643275.1:c.1064G= ENSP00000495598.1:n.1064G=
ENST00000643583.1:c.2575G= ENSP00000494685.1:p.Glu859=
ENST00000643625.1:c.467G= ENSP00000495546.1:n.467G=
ENST00000643875.1:c.2590G= ENSP00000495158.1:p.Glu864=
ENST00000644097.1:c.2587G= ENSP00000494682.1:p.Glu863=
ENST00000644184.1:c.1285G= ENSP00000495428.1:p.Glu429=
ENST00000644255.1:c.*2357G= ENSP00000493608.1:n.*2357G=
ENST00000644319.1:n.2965G=
ENST00000644786.1:n.249G=
ENST00000644882.1:n.1503G=
ENST00000645901.1:n.3441G=
ENST00000646391.1:c.*2360G= ENSP00000494104.1:n.*2360G=
ENST00000646625.1:c.2590G= ENSP00000496263.1:p.Glu864=
ENST00000647262.1:n.1555G=
ENST00000647279.1:c.*1829G= ENSP00000494502.1:n.*1829G=
ENST00000647506.1:n.3466G=
ENST00000647534.1:n.1654G=
ENST00000298552.7:c.2590G= ENSP00000298552.3:p.Glu864=
ENST00000440111.6:c.2590G= ENSP00000394524.2:p.Glu864=
ENST00000545250.5:c.2437G= ENSP00000444017.1:p.Glu813=
NM_000368.4:c.2590G= , LRG_486t1:c.2590G= NP_000359.1:p.Glu864=
NM_001162426.1:c.2587G= NP_001155898.1:p.Glu863=
NM_001162427.1:c.2437G= NP_001155899.1:p.Glu813=
XM_005272211.1:c.2590G= XP_005272268.1:p.Glu864=
XM_006717271.1:c.2590G= XP_006717334.1:p.Glu864=
XM_011518979.1:c.2590G= XP_011517281.1:p.Glu864=
NM_001362177.1:c.2227G= NP_001349106.1:p.Glu743=
XM_011518979.2:c.2590G= XP_011517281.1:p.Glu864=
XM_017015096.1:c.2590G= XP_016870585.1:p.Glu864=
XM_017015097.1:c.2590G= XP_016870586.1:p.Glu864=
XM_017015098.1:c.2587G= XP_016870587.1:p.Glu863=
XM_017015100.1:c.2227G= XP_016870589.1:p.Glu743=
XM_017015101.1:c.2224G= XP_016870590.1:p.Glu742=
NM_000368.5:c.2590G= MANE Select NP_000359.1:p.Glu864=
NM_001162426.2:c.2587G= NP_001155898.1:p.Glu863=
NM_001162427.2:c.2437G= NP_001155899.1:p.Glu813=
NM_001362177.2:c.2227G= NP_001349106.1:p.Glu743=