Canonical Allele Identifier: CA375358826
Community Standard Title: NM_000368.5(TSC1):c.2393C>T (p.Thr798Met)
Gene: TSC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.132901698G>A , CM000671.2:g.132901698G>A GRCh38
NC_000009.11:g.135777085G>A , CM000671.1:g.135777085G>A GRCh37
NC_000009.10:g.134766906G>A NCBI36
NG_012386.1:g.47936C>T , LRG_486:g.47936C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000368.5:c.2393C>T MANE Select NP_000359.1:p.Thr798Met
ENST00000298552.9:c.2393C>T MANE Select ENSP00000298552.3:p.Thr798Met
NM_000368.4:c.2393C>T , LRG_486t1:c.2393C>T NP_000359.1:p.Thr798Met
NM_001162426.1:c.2390C>T NP_001155898.1:p.Thr797Met
NM_001162426.2:c.2390C>T NP_001155898.1:p.Thr797Met
NM_001162427.1:c.2240C>T NP_001155899.1:p.Thr747Met
NM_001162427.2:c.2240C>T NP_001155899.1:p.Thr747Met
NM_001362177.1:c.2030C>T NP_001349106.1:p.Thr677Met
NM_001362177.2:c.2030C>T NP_001349106.1:p.Thr677Met
ENST00000298552.7:c.2393C>T ENSP00000298552.3:p.Thr798Met
ENST00000440111.6:c.2393C>T ENSP00000394524.2:p.Thr798Met
ENST00000475903.7:c.2390C>T ENSP00000496126.2:p.Thr797Met
ENST00000490179.4:c.2393C>T ENSP00000495533.2:p.Thr798Met
ENST00000545250.5:c.2240C>T ENSP00000444017.1:p.Thr747Met
ENST00000642261.1:c.453C>T
ENST00000642261.2:c.*172C>T ENSP00000494743.2:n.*172C>T
ENST00000642617.1:c.2390C>T ENSP00000493773.1:p.Thr797Met
ENST00000642627.1:c.2375C>T ENSP00000496772.1:p.Thr792Met
ENST00000642811.1:c.*2163C>T ENSP00000495554.1:n.*2163C>T
ENST00000643072.1:c.2240C>T ENSP00000496691.1:p.Thr747Met
ENST00000643275.1:c.867C>T ENSP00000495598.1:n.867C>T
ENST00000643275.2:c.*333C>T ENSP00000495598.2:n.*333C>T
ENST00000643362.2:c.2006C>T ENSP00000496398.2:p.Thr669Met
ENST00000643583.1:c.2378C>T ENSP00000494685.1:p.Thr793Met
ENST00000643625.1:c.270C>T ENSP00000495546.1:n.270C>T
ENST00000643625.2:c.*135C>T ENSP00000495546.2:n.*135C>T
ENST00000643691.2:c.2030C>T ENSP00000494916.2:p.Thr677Met
ENST00000643875.1:c.2393C>T ENSP00000495158.1:p.Thr798Met
ENST00000644097.1:c.2390C>T ENSP00000494682.1:p.Thr797Met
ENST00000644184.1:c.1130C>T ENSP00000495428.1:p.Thr377Met
ENST00000644184.2:c.2393C>T ENSP00000495428.2:p.Thr798Met
ENST00000644255.1:c.*2160C>T ENSP00000493608.1:n.*2160C>T
ENST00000644319.1:n.2768C>T
ENST00000644786.1:n.52C>T
ENST00000644882.1:n.1348C>T
ENST00000645129.2:c.2237C>T ENSP00000493639.2:p.Thr746Met
ENST00000645901.1:n.3244C>T
ENST00000646391.1:c.*2163C>T ENSP00000494104.1:n.*2163C>T
ENST00000646440.2:c.2393C>T ENSP00000495830.2:p.Thr798Met
ENST00000646625.1:c.2393C>T ENSP00000496263.1:p.Thr798Met
ENST00000647262.1:n.1358C>T
ENST00000647279.1:c.*1632C>T ENSP00000494502.1:n.*1632C>T
ENST00000647506.1:n.3269C>T
ENST00000647534.1:n.1457C>T
XM_005272211.1:c.2393C>T XP_005272268.1:p.Thr798Met
XM_006717271.1:c.2393C>T XP_006717334.1:p.Thr798Met
XM_011518979.1:c.2393C>T XP_011517281.1:p.Thr798Met
XM_011518979.2:c.2393C>T XP_011517281.1:p.Thr798Met
XM_017015096.1:c.2393C>T XP_016870585.1:p.Thr798Met
XM_017015097.1:c.2393C>T XP_016870586.1:p.Thr798Met
XM_017015098.1:c.2390C>T XP_016870587.1:p.Thr797Met
XM_017015100.1:c.2030C>T XP_016870589.1:p.Thr677Met
XM_017015101.1:c.2027C>T XP_016870590.1:p.Thr676Met