Canonical Allele Identifier: CA1882415084
Gene: TSC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.132896294C= , CM000671.2:g.132896294C= GRCh38
NC_000009.11:g.135771681C= , CM000671.1:g.135771681C= GRCh37
NC_000009.10:g.134761502C= NCBI36
NG_012386.1:g.53340G= , LRG_486:g.53340G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000475903.7:c.3433G= ENSP00000496126.2:p.Asp1145=
ENST00000490179.4:c.3436G= ENSP00000495533.2:p.Asp1146=
ENST00000642261.2:c.*1292G= ENSP00000494743.2:n.*1292G=
ENST00000643275.2:c.*1376G= ENSP00000495598.2:n.*1376G=
ENST00000643362.2:c.3049G= ENSP00000496398.2:p.Asp1017=
ENST00000643625.2:c.*1178G= ENSP00000495546.2:n.*1178G=
ENST00000643691.2:c.3073G= ENSP00000494916.2:p.Asp1025=
ENST00000644184.2:c.3394G= ENSP00000495428.2:p.Asp1132=
ENST00000645129.2:c.3280G= ENSP00000493639.2:p.Asp1094=
ENST00000646440.2:c.3436G= ENSP00000495830.2:p.Asp1146=
ENST00000298552.9:c.3436G= MANE Select ENSP00000298552.3:p.Asp1146=
ENST00000642617.1:c.3433G= ENSP00000493773.1:p.Asp1145=
ENST00000642627.1:c.3418G= ENSP00000496772.1:p.Asp1140=
ENST00000642811.1:c.*3206G= ENSP00000495554.1:n.*3206G=
ENST00000643072.1:c.3283G= ENSP00000496691.1:p.Asp1095=
ENST00000643583.1:c.3421G= ENSP00000494685.1:p.Asp1141=
ENST00000643625.1:c.1313G= ENSP00000495546.1:n.1313G=
ENST00000643875.1:c.3436G= ENSP00000495158.1:p.Asp1146=
ENST00000644097.1:c.3433G= ENSP00000494682.1:p.Asp1145=
ENST00000644184.1:c.2131G= ENSP00000495428.1:p.Asp711=
ENST00000644255.1:c.*3203G= ENSP00000493608.1:n.*3203G=
ENST00000644319.1:n.3811G=
ENST00000644786.1:n.1095G=
ENST00000644882.1:n.2344G=
ENST00000645901.1:n.4287G=
ENST00000646391.1:c.*3206G= ENSP00000494104.1:n.*3206G=
ENST00000646625.1:c.3436G= ENSP00000496263.1:p.Asp1146=
ENST00000647262.1:n.2401G=
ENST00000647279.1:c.*2675G= ENSP00000494502.1:n.*2675G=
ENST00000647534.1:n.2500G=
ENST00000298552.7:c.3436G= ENSP00000298552.3:p.Asp1146=
ENST00000440111.6:c.3436G= ENSP00000394524.2:p.Asp1146=
ENST00000545250.5:c.3283G= ENSP00000444017.1:p.Asp1095=
NM_000368.4:c.3436G= , LRG_486t1:c.3436G= NP_000359.1:p.Asp1146=
NM_001162426.1:c.3433G= NP_001155898.1:p.Asp1145=
NM_001162427.1:c.3283G= NP_001155899.1:p.Asp1095=
XM_005272211.1:c.3436G= XP_005272268.1:p.Asp1146=
XM_006717271.1:c.3436G= XP_006717334.1:p.Asp1146=
XM_011518979.1:c.3436G= XP_011517281.1:p.Asp1146=
NM_001362177.1:c.3073G= NP_001349106.1:p.Asp1025=
XM_011518979.2:c.3436G= XP_011517281.1:p.Asp1146=
XM_017015096.1:c.3436G= XP_016870585.1:p.Asp1146=
XM_017015097.1:c.3436G= XP_016870586.1:p.Asp1146=
XM_017015098.1:c.3433G= XP_016870587.1:p.Asp1145=
XM_017015100.1:c.3073G= XP_016870589.1:p.Asp1025=
XM_017015101.1:c.3070G= XP_016870590.1:p.Asp1024=
NM_000368.5:c.3436G= MANE Select NP_000359.1:p.Asp1146=
NM_001162426.2:c.3433G= NP_001155898.1:p.Asp1145=
NM_001162427.2:c.3283G= NP_001155899.1:p.Asp1095=
NM_001362177.2:c.3073G= NP_001349106.1:p.Asp1025=