Canonical Allele Identifier: CA1882415260
Gene: TSC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.132896330T= , CM000671.2:g.132896330T= GRCh38
NC_000009.11:g.135771717T= , CM000671.1:g.135771717T= GRCh37
NC_000009.10:g.134761538T= NCBI36
NG_012386.1:g.53304A= , LRG_486:g.53304A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000475903.7:c.3397A= ENSP00000496126.2:p.Asn1133=
ENST00000490179.4:c.3400A= ENSP00000495533.2:p.Asn1134=
ENST00000642261.2:c.*1256A= ENSP00000494743.2:n.*1256A=
ENST00000643275.2:c.*1340A= ENSP00000495598.2:n.*1340A=
ENST00000643362.2:c.3013A= ENSP00000496398.2:p.Asn1005=
ENST00000643625.2:c.*1142A= ENSP00000495546.2:n.*1142A=
ENST00000643691.2:c.3037A= ENSP00000494916.2:p.Asn1013=
ENST00000644184.2:c.3358A= ENSP00000495428.2:p.Asn1120=
ENST00000645129.2:c.3244A= ENSP00000493639.2:p.Asn1082=
ENST00000646440.2:c.3400A= ENSP00000495830.2:p.Asn1134=
ENST00000298552.9:c.3400A= MANE Select ENSP00000298552.3:p.Asn1134=
ENST00000642617.1:c.3397A= ENSP00000493773.1:p.Asn1133=
ENST00000642627.1:c.3382A= ENSP00000496772.1:p.Asn1128=
ENST00000642811.1:c.*3170A= ENSP00000495554.1:n.*3170A=
ENST00000643072.1:c.3247A= ENSP00000496691.1:p.Asn1083=
ENST00000643583.1:c.3385A= ENSP00000494685.1:p.Asn1129=
ENST00000643625.1:c.1277A= ENSP00000495546.1:n.1277A=
ENST00000643875.1:c.3400A= ENSP00000495158.1:p.Asn1134=
ENST00000644097.1:c.3397A= ENSP00000494682.1:p.Asn1133=
ENST00000644184.1:c.2095A= ENSP00000495428.1:p.Asn699=
ENST00000644255.1:c.*3167A= ENSP00000493608.1:n.*3167A=
ENST00000644319.1:n.3775A=
ENST00000644786.1:n.1059A=
ENST00000644882.1:n.2308A=
ENST00000645901.1:n.4251A=
ENST00000646391.1:c.*3170A= ENSP00000494104.1:n.*3170A=
ENST00000646625.1:c.3400A= ENSP00000496263.1:p.Asn1134=
ENST00000647262.1:n.2365A=
ENST00000647279.1:c.*2639A= ENSP00000494502.1:n.*2639A=
ENST00000647534.1:n.2464A=
ENST00000298552.7:c.3400A= ENSP00000298552.3:p.Asn1134=
ENST00000440111.6:c.3400A= ENSP00000394524.2:p.Asn1134=
ENST00000545250.5:c.3247A= ENSP00000444017.1:p.Asn1083=
NM_000368.4:c.3400A= , LRG_486t1:c.3400A= NP_000359.1:p.Asn1134=
NM_001162426.1:c.3397A= NP_001155898.1:p.Asn1133=
NM_001162427.1:c.3247A= NP_001155899.1:p.Asn1083=
XM_005272211.1:c.3400A= XP_005272268.1:p.Asn1134=
XM_006717271.1:c.3400A= XP_006717334.1:p.Asn1134=
XM_011518979.1:c.3400A= XP_011517281.1:p.Asn1134=
NM_001362177.1:c.3037A= NP_001349106.1:p.Asn1013=
XM_011518979.2:c.3400A= XP_011517281.1:p.Asn1134=
XM_017015096.1:c.3400A= XP_016870585.1:p.Asn1134=
XM_017015097.1:c.3400A= XP_016870586.1:p.Asn1134=
XM_017015098.1:c.3397A= XP_016870587.1:p.Asn1133=
XM_017015100.1:c.3037A= XP_016870589.1:p.Asn1013=
XM_017015101.1:c.3034A= XP_016870590.1:p.Asn1012=
NM_000368.5:c.3400A= MANE Select NP_000359.1:p.Asn1134=
NM_001162426.2:c.3397A= NP_001155898.1:p.Asn1133=
NM_001162427.2:c.3247A= NP_001155899.1:p.Asn1083=
NM_001362177.2:c.3037A= NP_001349106.1:p.Asn1013=