Canonical Allele Identifier: CA1882410756
Gene: TSC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.132903683C= , CM000671.2:g.132903683C= GRCh38
NC_000009.11:g.135779070C= , CM000671.1:g.135779070C= GRCh37
NC_000009.10:g.134768891C= NCBI36
NG_012386.1:g.45951G= , LRG_486:g.45951G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000475903.7:c.2173G= ENSP00000496126.2:p.Ala725=
ENST00000490179.4:c.2176G= ENSP00000495533.2:p.Ala726=
ENST00000642261.2:c.2176G= ENSP00000494743.2:p.Ala726=
ENST00000643275.2:c.*116G= ENSP00000495598.2:n.*116G=
ENST00000643362.2:c.1789G= ENSP00000496398.2:p.Ala597=
ENST00000643625.2:c.2041+728G= ENSP00000495546.2:n.2041+728G=
ENST00000643691.2:c.1813G= ENSP00000494916.2:p.Ala605=
ENST00000644184.2:c.2176G= ENSP00000495428.2:p.Ala726=
ENST00000645129.2:c.2020G= ENSP00000493639.2:p.Ala674=
ENST00000646440.2:c.2176G= ENSP00000495830.2:p.Ala726=
ENST00000298552.9:c.2176G= MANE Select ENSP00000298552.3:p.Ala726=
ENST00000642261.1:c.240G=
ENST00000642617.1:c.2173G= ENSP00000493773.1:p.Ala725=
ENST00000642627.1:c.2158G= ENSP00000496772.1:p.Ala720=
ENST00000642811.1:c.*1946G= ENSP00000495554.1:n.*1946G=
ENST00000643072.1:c.2023G= ENSP00000496691.1:p.Ala675=
ENST00000643275.1:c.650G= ENSP00000495598.1:n.650G=
ENST00000643583.1:c.2161G= ENSP00000494685.1:p.Ala721=
ENST00000643625.1:c.85+728G= ENSP00000495546.1:n.85+728G=
ENST00000643875.1:c.2176G= ENSP00000495158.1:p.Ala726=
ENST00000644097.1:c.2173G= ENSP00000494682.1:p.Ala725=
ENST00000644184.1:c.913G= ENSP00000495428.1:p.Ala305=
ENST00000644255.1:c.*1943G= ENSP00000493608.1:n.*1943G=
ENST00000644319.1:n.2551G=
ENST00000644882.1:n.1131G=
ENST00000645901.1:n.3027G=
ENST00000646391.1:c.*1946G= ENSP00000494104.1:n.*1946G=
ENST00000646625.1:c.2176G= ENSP00000496263.1:p.Ala726=
ENST00000647262.1:n.1141G=
ENST00000647279.1:c.*1415G= ENSP00000494502.1:n.*1415G=
ENST00000647506.1:n.3052G=
ENST00000647534.1:n.1240G=
ENST00000298552.7:c.2176G= ENSP00000298552.3:p.Ala726=
ENST00000440111.6:c.2176G= ENSP00000394524.2:p.Ala726=
ENST00000545250.5:c.2023G= ENSP00000444017.1:p.Ala675=
NM_000368.4:c.2176G= , LRG_486t1:c.2176G= NP_000359.1:p.Ala726=
NM_001162426.1:c.2173G= NP_001155898.1:p.Ala725=
NM_001162427.1:c.2023G= NP_001155899.1:p.Ala675=
XM_005272211.1:c.2176G= XP_005272268.1:p.Ala726=
XM_006717271.1:c.2176G= XP_006717334.1:p.Ala726=
XM_011518979.1:c.2176G= XP_011517281.1:p.Ala726=
NM_001362177.1:c.1813G= NP_001349106.1:p.Ala605=
XM_011518979.2:c.2176G= XP_011517281.1:p.Ala726=
XM_017015096.1:c.2176G= XP_016870585.1:p.Ala726=
XM_017015097.1:c.2176G= XP_016870586.1:p.Ala726=
XM_017015098.1:c.2173G= XP_016870587.1:p.Ala725=
XM_017015100.1:c.1813G= XP_016870589.1:p.Ala605=
XM_017015101.1:c.1810G= XP_016870590.1:p.Ala604=
NM_000368.5:c.2176G= MANE Select NP_000359.1:p.Ala726=
NM_001162426.2:c.2173G= NP_001155898.1:p.Ala725=
NM_001162427.2:c.2023G= NP_001155899.1:p.Ala675=
NM_001362177.2:c.1813G= NP_001349106.1:p.Ala605=