Canonical Allele Identifier: CA1882410717
Gene: TSC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.132903678T= , CM000671.2:g.132903678T= GRCh38
NC_000009.11:g.135779065T= , CM000671.1:g.135779065T= GRCh37
NC_000009.10:g.134768886T= NCBI36
NG_012386.1:g.45956A= , LRG_486:g.45956A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000475903.7:c.2178A= ENSP00000496126.2:p.Ala726=
ENST00000490179.4:c.2181A= ENSP00000495533.2:p.Ala727=
ENST00000642261.2:c.2181A= ENSP00000494743.2:p.Ala727=
ENST00000643275.2:c.*121A= ENSP00000495598.2:n.*121A=
ENST00000643362.2:c.1794A= ENSP00000496398.2:p.Ala598=
ENST00000643625.2:c.2041+733A= ENSP00000495546.2:n.2041+733A=
ENST00000643691.2:c.1818A= ENSP00000494916.2:p.Ala606=
ENST00000644184.2:c.2181A= ENSP00000495428.2:p.Ala727=
ENST00000645129.2:c.2025A= ENSP00000493639.2:p.Ala675=
ENST00000646440.2:c.2181A= ENSP00000495830.2:p.Ala727=
ENST00000298552.9:c.2181A= MANE Select ENSP00000298552.3:p.Ala727=
ENST00000642261.1:c.245A=
ENST00000642617.1:c.2178A= ENSP00000493773.1:p.Ala726=
ENST00000642627.1:c.2163A= ENSP00000496772.1:p.Ala721=
ENST00000642811.1:c.*1951A= ENSP00000495554.1:n.*1951A=
ENST00000643072.1:c.2028A= ENSP00000496691.1:p.Ala676=
ENST00000643275.1:c.655A= ENSP00000495598.1:n.655A=
ENST00000643583.1:c.2166A= ENSP00000494685.1:p.Ala722=
ENST00000643625.1:c.85+733A= ENSP00000495546.1:n.85+733A=
ENST00000643875.1:c.2181A= ENSP00000495158.1:p.Ala727=
ENST00000644097.1:c.2178A= ENSP00000494682.1:p.Ala726=
ENST00000644184.1:c.918A= ENSP00000495428.1:p.Ala306=
ENST00000644255.1:c.*1948A= ENSP00000493608.1:n.*1948A=
ENST00000644319.1:n.2556A=
ENST00000644882.1:n.1136A=
ENST00000645901.1:n.3032A=
ENST00000646391.1:c.*1951A= ENSP00000494104.1:n.*1951A=
ENST00000646625.1:c.2181A= ENSP00000496263.1:p.Ala727=
ENST00000647262.1:n.1146A=
ENST00000647279.1:c.*1420A= ENSP00000494502.1:n.*1420A=
ENST00000647506.1:n.3057A=
ENST00000647534.1:n.1245A=
ENST00000298552.7:c.2181A= ENSP00000298552.3:p.Ala727=
ENST00000440111.6:c.2181A= ENSP00000394524.2:p.Ala727=
ENST00000545250.5:c.2028A= ENSP00000444017.1:p.Ala676=
NM_000368.4:c.2181A= , LRG_486t1:c.2181A= NP_000359.1:p.Ala727=
NM_001162426.1:c.2178A= NP_001155898.1:p.Ala726=
NM_001162427.1:c.2028A= NP_001155899.1:p.Ala676=
XM_005272211.1:c.2181A= XP_005272268.1:p.Ala727=
XM_006717271.1:c.2181A= XP_006717334.1:p.Ala727=
XM_011518979.1:c.2181A= XP_011517281.1:p.Ala727=
NM_001362177.1:c.1818A= NP_001349106.1:p.Ala606=
XM_011518979.2:c.2181A= XP_011517281.1:p.Ala727=
XM_017015096.1:c.2181A= XP_016870585.1:p.Ala727=
XM_017015097.1:c.2181A= XP_016870586.1:p.Ala727=
XM_017015098.1:c.2178A= XP_016870587.1:p.Ala726=
XM_017015100.1:c.1818A= XP_016870589.1:p.Ala606=
XM_017015101.1:c.1815A= XP_016870590.1:p.Ala605=
NM_000368.5:c.2181A= MANE Select NP_000359.1:p.Ala727=
NM_001162426.2:c.2178A= NP_001155898.1:p.Ala726=
NM_001162427.2:c.2028A= NP_001155899.1:p.Ala676=
NM_001362177.2:c.1818A= NP_001349106.1:p.Ala606=