Canonical Allele Identifier: CA1882405872
Gene: TSC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.132900735T= , CM000671.2:g.132900735T= GRCh38
NC_000009.11:g.135776122T= , CM000671.1:g.135776122T= GRCh37
NC_000009.10:g.134765943T= NCBI36
NG_012386.1:g.48899A= , LRG_486:g.48899A=

Transcript Alleles

HGVS Amino-acid change
ENST00000475903.7:c.2602A= ENSP00000496126.2:p.Lys868=
ENST00000490179.4:c.2605A= ENSP00000495533.2:p.Lys869=
ENST00000642261.2:c.*384A= ENSP00000494743.2:n.*384A=
ENST00000643275.2:c.*545A= ENSP00000495598.2:n.*545A=
ENST00000643362.2:c.2218A= ENSP00000496398.2:p.Lys740=
ENST00000643625.2:c.*347A= ENSP00000495546.2:n.*347A=
ENST00000643691.2:c.2242A= ENSP00000494916.2:p.Lys748=
ENST00000644184.2:c.2563A= ENSP00000495428.2:p.Lys855=
ENST00000645129.2:c.2449A= ENSP00000493639.2:p.Lys817=
ENST00000646440.2:c.2605A= ENSP00000495830.2:p.Lys869=
ENST00000298552.9:c.2605A= MANE Select ENSP00000298552.3:p.Lys869=
ENST00000642261.1:c.665A=
ENST00000642617.1:c.2602A= ENSP00000493773.1:p.Lys868=
ENST00000642627.1:c.2587A= ENSP00000496772.1:p.Lys863=
ENST00000642811.1:c.*2375A= ENSP00000495554.1:n.*2375A=
ENST00000643072.1:c.2452A= ENSP00000496691.1:p.Lys818=
ENST00000643275.1:c.1079A= ENSP00000495598.1:n.1079A=
ENST00000643583.1:c.2590A= ENSP00000494685.1:p.Lys864=
ENST00000643625.1:c.482A= ENSP00000495546.1:n.482A=
ENST00000643875.1:c.2605A= ENSP00000495158.1:p.Lys869=
ENST00000644097.1:c.2602A= ENSP00000494682.1:p.Lys868=
ENST00000644184.1:c.1300A= ENSP00000495428.1:p.Lys434=
ENST00000644255.1:c.*2372A= ENSP00000493608.1:n.*2372A=
ENST00000644319.1:n.2980A=
ENST00000644786.1:n.264A=
ENST00000644882.1:n.1518A=
ENST00000645901.1:n.3456A=
ENST00000646391.1:c.*2375A= ENSP00000494104.1:n.*2375A=
ENST00000646625.1:c.2605A= ENSP00000496263.1:p.Lys869=
ENST00000647262.1:n.1570A=
ENST00000647279.1:c.*1844A= ENSP00000494502.1:n.*1844A=
ENST00000647506.1:n.3481A=
ENST00000647534.1:n.1669A=
ENST00000298552.7:c.2605A= ENSP00000298552.3:p.Lys869=
ENST00000440111.6:c.2605A= ENSP00000394524.2:p.Lys869=
ENST00000545250.5:c.2452A= ENSP00000444017.1:p.Lys818=
NM_000368.4:c.2605A= , LRG_486t1:c.2605A= NP_000359.1:p.Lys869=
NM_001162426.1:c.2602A= NP_001155898.1:p.Lys868=
NM_001162427.1:c.2452A= NP_001155899.1:p.Lys818=
XM_005272211.1:c.2605A= XP_005272268.1:p.Lys869=
XM_006717271.1:c.2605A= XP_006717334.1:p.Lys869=
XM_011518979.1:c.2605A= XP_011517281.1:p.Lys869=
NM_001362177.1:c.2242A= NP_001349106.1:p.Lys748=
XM_011518979.2:c.2605A= XP_011517281.1:p.Lys869=
XM_017015096.1:c.2605A= XP_016870585.1:p.Lys869=
XM_017015097.1:c.2605A= XP_016870586.1:p.Lys869=
XM_017015098.1:c.2602A= XP_016870587.1:p.Lys868=
XM_017015100.1:c.2242A= XP_016870589.1:p.Lys748=
XM_017015101.1:c.2239A= XP_016870590.1:p.Lys747=
NM_000368.5:c.2605A= MANE Select NP_000359.1:p.Lys869=
NM_001162426.2:c.2602A= NP_001155898.1:p.Lys868=
NM_001162427.2:c.2452A= NP_001155899.1:p.Lys818=
NM_001362177.2:c.2242A= NP_001349106.1:p.Lys748=