Canonical Allele Identifier: CA1139661269
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 945513
ClinVar RCV Id: RCV001216170

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.132902733_132903997del , CM000671.2:g.132902733_132903997del GRCh38
NC_000009.11:g.135778120_135779384del , CM000671.1:g.135778120_135779384del GRCh37
NC_000009.10:g.134767941_134769205del NCBI36
NG_012386.1:g.45640_46904del , LRG_486:g.45640_46904del

Transcript Alleles

HGVS Amino-acid change
ENST00000475903.7:c.2039-177_2263del
ENST00000490179.4:c.2042-177_2266del
ENST00000642261.2:c.2042-177_*45del
ENST00000643275.2:c.1998-177_*206del
ENST00000643362.2:c.1655-177_1879del
ENST00000643625.2:c.2041+417_*8del
ENST00000643691.2:c.1679-177_1903del
ENST00000644184.2:c.2042-177_2266del
ENST00000645129.2:c.1886-177_2110del
ENST00000646440.2:c.2042-177_2266del
ENST00000298552.9:c.2042-177_2266del
ENST00000642261.1:c.106-177_326del
ENST00000642617.1:c.2039-177_2263del
ENST00000642627.1:c.2039-192_2248del
ENST00000642811.1:c.*1812-177_*2036del
ENST00000643072.1:c.1889-177_2113del
ENST00000643275.1:c.516-177_740del
ENST00000643583.1:c.2042-192_2251del
ENST00000643625.1:c.85+417_143del
ENST00000643875.1:c.2042-177_2266del
ENST00000644097.1:c.2039-177_2263del
ENST00000644184.1:c.779-177_1003del
ENST00000644255.1:c.*1809-177_*2033del
ENST00000644319.1:n.2417-177_2641del
ENST00000644882.1:n.997-177_1221del
ENST00000645901.1:n.2893-177_3117del
ENST00000646391.1:c.*1812-177_*2036del
ENST00000646625.1:c.2042-177_2266del
ENST00000647262.1:n.1007-177_1231del
ENST00000647279.1:c.*1281-177_*1505del
ENST00000647506.1:n.2918-177_3142del
ENST00000647534.1:n.1106-177_1330del
ENST00000298552.7:c.2042-177_2266del
ENST00000440111.6:c.2042-177_2266del
ENST00000545250.5:c.1889-177_2113del
NM_000368.4:c.2042-177_2266del , LRG_486t1:c.2042-177_2266del
NM_001162426.1:c.2039-177_2263del
NM_001162427.1:c.1889-177_2113del
XM_005272211.1:c.2042-177_2266del
XM_006717271.1:c.2042-177_2266del
XM_011518979.1:c.2042-177_2266del
NM_001362177.1:c.1679-177_1903del
XM_011518979.2:c.2042-177_2266del
XM_017015096.1:c.2042-177_2266del
XM_017015097.1:c.2042-177_2266del
XM_017015098.1:c.2039-177_2263del
XM_017015100.1:c.1679-177_1903del
XM_017015101.1:c.1676-177_1900del
NM_000368.5:c.2042-177_2266del
NM_001162426.2:c.2039-177_2263del
NM_001162427.2:c.1889-177_2113del
NM_001362177.2:c.1679-177_1903del