Canonical Allele Identifier: CA1882405921
Gene: TSC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.132900755T= , CM000671.2:g.132900755T= GRCh38
NC_000009.11:g.135776142T= , CM000671.1:g.135776142T= GRCh37
NC_000009.10:g.134765963T= NCBI36
NG_012386.1:g.48879A= , LRG_486:g.48879A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000475903.7:c.2582A= ENSP00000496126.2:p.Tyr861=
ENST00000490179.4:c.2585A= ENSP00000495533.2:p.Tyr862=
ENST00000642261.2:c.*364A= ENSP00000494743.2:n.*364A=
ENST00000643275.2:c.*525A= ENSP00000495598.2:n.*525A=
ENST00000643362.2:c.2198A= ENSP00000496398.2:p.Tyr733=
ENST00000643625.2:c.*327A= ENSP00000495546.2:n.*327A=
ENST00000643691.2:c.2222A= ENSP00000494916.2:p.Tyr741=
ENST00000644184.2:c.2543A= ENSP00000495428.2:p.Tyr848=
ENST00000645129.2:c.2429A= ENSP00000493639.2:p.Tyr810=
ENST00000646440.2:c.2585A= ENSP00000495830.2:p.Tyr862=
ENST00000298552.9:c.2585A= MANE Select ENSP00000298552.3:p.Tyr862=
ENST00000642261.1:c.645A=
ENST00000642617.1:c.2582A= ENSP00000493773.1:p.Tyr861=
ENST00000642627.1:c.2567A= ENSP00000496772.1:p.Tyr856=
ENST00000642811.1:c.*2355A= ENSP00000495554.1:n.*2355A=
ENST00000643072.1:c.2432A= ENSP00000496691.1:p.Tyr811=
ENST00000643275.1:c.1059A= ENSP00000495598.1:n.1059A=
ENST00000643583.1:c.2570A= ENSP00000494685.1:p.Tyr857=
ENST00000643625.1:c.462A= ENSP00000495546.1:n.462A=
ENST00000643875.1:c.2585A= ENSP00000495158.1:p.Tyr862=
ENST00000644097.1:c.2582A= ENSP00000494682.1:p.Tyr861=
ENST00000644184.1:c.1280A= ENSP00000495428.1:p.Tyr427=
ENST00000644255.1:c.*2352A= ENSP00000493608.1:n.*2352A=
ENST00000644319.1:n.2960A=
ENST00000644786.1:n.244A=
ENST00000644882.1:n.1498A=
ENST00000645901.1:n.3436A=
ENST00000646391.1:c.*2355A= ENSP00000494104.1:n.*2355A=
ENST00000646625.1:c.2585A= ENSP00000496263.1:p.Tyr862=
ENST00000647262.1:n.1550A=
ENST00000647279.1:c.*1824A= ENSP00000494502.1:n.*1824A=
ENST00000647506.1:n.3461A=
ENST00000647534.1:n.1649A=
ENST00000298552.7:c.2585A= ENSP00000298552.3:p.Tyr862=
ENST00000440111.6:c.2585A= ENSP00000394524.2:p.Tyr862=
ENST00000545250.5:c.2432A= ENSP00000444017.1:p.Tyr811=
NM_000368.4:c.2585A= , LRG_486t1:c.2585A= NP_000359.1:p.Tyr862=
NM_001162426.1:c.2582A= NP_001155898.1:p.Tyr861=
NM_001162427.1:c.2432A= NP_001155899.1:p.Tyr811=
XM_005272211.1:c.2585A= XP_005272268.1:p.Tyr862=
XM_006717271.1:c.2585A= XP_006717334.1:p.Tyr862=
XM_011518979.1:c.2585A= XP_011517281.1:p.Tyr862=
NM_001362177.1:c.2222A= NP_001349106.1:p.Tyr741=
XM_011518979.2:c.2585A= XP_011517281.1:p.Tyr862=
XM_017015096.1:c.2585A= XP_016870585.1:p.Tyr862=
XM_017015097.1:c.2585A= XP_016870586.1:p.Tyr862=
XM_017015098.1:c.2582A= XP_016870587.1:p.Tyr861=
XM_017015100.1:c.2222A= XP_016870589.1:p.Tyr741=
XM_017015101.1:c.2219A= XP_016870590.1:p.Tyr740=
NM_000368.5:c.2585A= MANE Select NP_000359.1:p.Tyr862=
NM_001162426.2:c.2582A= NP_001155898.1:p.Tyr861=
NM_001162427.2:c.2432A= NP_001155899.1:p.Tyr811=
NM_001362177.2:c.2222A= NP_001349106.1:p.Tyr741=