Canonical Allele Identifier: CA1882405260

Gene: TSC1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132900254_132900257delinsAATT , CM000671.2:g.132900254_132900257delinsAATT	GRCh38
NC_000009.11:g.135775641_135775644delinsAATT , CM000671.1:g.135775641_135775644delinsAATT	GRCh37
NC_000009.10:g.134765462_134765465delinsAATT	NCBI36
NG_012386.1:g.49377_49380delinsAATT , LRG_486:g.49377_49380delinsAATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475903.7:c.2622+458_2622+461delinsAATT	ENSP00000496126.2:n.2622+458_2622+461delinsAATT
ENST00000490179.4:c.2625+458_2625+461delinsAATT	ENSP00000495533.2:n.2625+458_2625+461delinsAATT
ENST00000642261.2:c.*404+458_*404+461delinsAATT	ENSP00000494743.2:n.*404+458_*404+461delinsAATT
ENST00000643275.2:c.*565+458_*565+461delinsAATT	ENSP00000495598.2:n.*565+458_*565+461delinsAATT
ENST00000643362.2:c.2238+458_2238+461delinsAATT	ENSP00000496398.2:n.2238+458_2238+461delinsAATT
ENST00000643625.2:c.*367+458_*367+461delinsAATT	ENSP00000495546.2:n.*367+458_*367+461delinsAATT
ENST00000643691.2:c.2262+458_2262+461delinsAATT	ENSP00000494916.2:n.2262+458_2262+461delinsAATT
ENST00000644184.2:c.2583+458_2583+461delinsAATT	ENSP00000495428.2:n.2583+458_2583+461delinsAATT
ENST00000645129.2:c.2469+458_2469+461delinsAATT	ENSP00000493639.2:n.2469+458_2469+461delinsAATT
ENST00000646440.2:c.2625+458_2625+461delinsAATT	ENSP00000495830.2:n.2625+458_2625+461delinsAATT
ENST00000298552.9:c.2625+458_2625+461delinsAATT MANE Select	ENSP00000298552.3:n.2625+458_2625+461delinsAATT
ENST00000642261.1:c.685+458_685+461delinsAATT
ENST00000642617.1:c.2622+458_2622+461delinsAATT	ENSP00000493773.1:n.2622+458_2622+461delinsAATT
ENST00000642627.1:c.2607+458_2607+461delinsAATT	ENSP00000496772.1:n.2607+458_2607+461delinsAATT
ENST00000642811.1:c.*2395+458_*2395+461delinsAATT	ENSP00000495554.1:n.*2395+458_*2395+461delinsAATT
ENST00000643072.1:c.2472+458_2472+461delinsAATT	ENSP00000496691.1:n.2472+458_2472+461delinsAATT
ENST00000643275.1:c.1099+458_1099+461delinsAATT	ENSP00000495598.1:n.1099+458_1099+461delinsAATT
ENST00000643583.1:c.2610+458_2610+461delinsAATT	ENSP00000494685.1:n.2610+458_2610+461delinsAATT
ENST00000643625.1:c.502+458_502+461delinsAATT	ENSP00000495546.1:n.502+458_502+461delinsAATT
ENST00000643875.1:c.2625+458_2625+461delinsAATT	ENSP00000495158.1:n.2625+458_2625+461delinsAATT
ENST00000644097.1:c.2622+458_2622+461delinsAATT	ENSP00000494682.1:n.2622+458_2622+461delinsAATT
ENST00000644184.1:c.1320+458_1320+461delinsAATT	ENSP00000495428.1:n.1320+458_1320+461delinsAATT
ENST00000644255.1:c.*2392+458_*2392+461delinsAATT	ENSP00000493608.1:n.*2392+458_*2392+461delinsAATT
ENST00000644319.1:n.3000+458_3000+461delinsAATT
ENST00000644786.1:n.284+458_284+461delinsAATT
ENST00000644882.1:n.1538+458_1538+461delinsAATT
ENST00000645901.1:n.3476+458_3476+461delinsAATT
ENST00000646391.1:c.*2395+458_*2395+461delinsAATT	ENSP00000494104.1:n.*2395+458_*2395+461delinsAATT
ENST00000646625.1:c.2625+458_2625+461delinsAATT	ENSP00000496263.1:n.2625+458_2625+461delinsAATT
ENST00000647262.1:n.1590+458_1590+461delinsAATT
ENST00000647279.1:c.*1864+458_*1864+461delinsAATT	ENSP00000494502.1:n.*1864+458_*1864+461delinsAATT
ENST00000647506.1:n.3959_3962delinsAATT
ENST00000647534.1:n.1689+458_1689+461delinsAATT
ENST00000298552.7:c.2625+458_2625+461delinsAATT	ENSP00000298552.3:n.2625+458_2625+461delinsAATT
ENST00000440111.6:c.2625+458_2625+461delinsAATT	ENSP00000394524.2:n.2625+458_2625+461delinsAATT
ENST00000545250.5:c.2472+458_2472+461delinsAATT	ENSP00000444017.1:n.2472+458_2472+461delinsAATT
NM_000368.4:c.2625+458_2625+461delinsAATT , LRG_486t1:c.2625+458_2625+461delinsAATT	NP_000359.1:n.2625+458_2625+461delinsAATT
NM_001162426.1:c.2622+458_2622+461delinsAATT	NP_001155898.1:n.2622+458_2622+461delinsAATT
NM_001162427.1:c.2472+458_2472+461delinsAATT	NP_001155899.1:n.2472+458_2472+461delinsAATT
XM_005272211.1:c.2625+458_2625+461delinsAATT	XP_005272268.1:n.2625+458_2625+461delinsAATT
XM_006717271.1:c.2625+458_2625+461delinsAATT	XP_006717334.1:n.2625+458_2625+461delinsAATT
XM_011518979.1:c.2625+458_2625+461delinsAATT	XP_011517281.1:n.2625+458_2625+461delinsAATT
NM_001362177.1:c.2262+458_2262+461delinsAATT	NP_001349106.1:n.2262+458_2262+461delinsAATT
XM_011518979.2:c.2625+458_2625+461delinsAATT	XP_011517281.1:n.2625+458_2625+461delinsAATT
XM_017015096.1:c.2625+458_2625+461delinsAATT	XP_016870585.1:n.2625+458_2625+461delinsAATT
XM_017015097.1:c.2625+458_2625+461delinsAATT	XP_016870586.1:n.2625+458_2625+461delinsAATT
XM_017015098.1:c.2622+458_2622+461delinsAATT	XP_016870587.1:n.2622+458_2622+461delinsAATT
XM_017015100.1:c.2262+458_2262+461delinsAATT	XP_016870589.1:n.2262+458_2262+461delinsAATT
XM_017015101.1:c.2259+458_2259+461delinsAATT	XP_016870590.1:n.2259+458_2259+461delinsAATT
NM_000368.5:c.2625+458_2625+461delinsAATT MANE Select	NP_000359.1:n.2625+458_2625+461delinsAATT
NM_001162426.2:c.2622+458_2622+461delinsAATT	NP_001155898.1:n.2622+458_2622+461delinsAATT
NM_001162427.2:c.2472+458_2472+461delinsAATT	NP_001155899.1:n.2472+458_2472+461delinsAATT
NM_001362177.2:c.2262+458_2262+461delinsAATT	NP_001349106.1:n.2262+458_2262+461delinsAATT