Canonical Allele Identifier: CA2720730089

Gene: TSC1

Linked Data

• dbSNP Id: rs2131876562

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132907252del , CM000671.2:g.132907252del	GRCh38
NC_000009.11:g.135782639del , CM000671.1:g.135782639del	GRCh37
NC_000009.10:g.134772460del	NCBI36
NG_012386.1:g.42383del , LRG_486:g.42383del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475903.7:c.1330+50del	ENSP00000496126.2:n.1330+50del
ENST00000490179.4:c.1333+50del	ENSP00000495533.2:n.1333+50del
ENST00000642261.2:c.1333+50del	ENSP00000494743.2:n.1333+50del
ENST00000643275.2:c.1333+50del	ENSP00000495598.2:n.1333+50del
ENST00000643362.2:c.946+50del	ENSP00000496398.2:n.946+50del
ENST00000643625.2:c.1333+50del	ENSP00000495546.2:n.1333+50del
ENST00000643691.2:c.970+50del	ENSP00000494916.2:n.970+50del
ENST00000644184.2:c.1333+50del	ENSP00000495428.2:n.1333+50del
ENST00000645129.2:c.1177+50del	ENSP00000493639.2:n.1177+50del
ENST00000646440.2:c.1333+50del	ENSP00000495830.2:n.1333+50del
ENST00000298552.9:c.1333+50del MANE Select	ENSP00000298552.3:n.1333+50del
ENST00000642344.1:c.*1074+50del	ENSP00000494847.1:n.*1074+50del
ENST00000642617.1:c.1330+50del	ENSP00000493773.1:n.1330+50del
ENST00000642627.1:c.1330+50del	ENSP00000496772.1:n.1330+50del
ENST00000642811.1:c.*1103+50del	ENSP00000495554.1:n.*1103+50del
ENST00000643072.1:c.1180+50del	ENSP00000496691.1:n.1180+50del
ENST00000643362.1:c.946+50del	ENSP00000496398.1:n.946+50del
ENST00000643583.1:c.1333+50del	ENSP00000494685.1:n.1333+50del
ENST00000643875.1:c.1333+50del	ENSP00000495158.1:n.1333+50del
ENST00000644097.1:c.1330+50del	ENSP00000494682.1:n.1330+50del
ENST00000644184.1:c.70+50del	ENSP00000495428.1:n.70+50del
ENST00000644255.1:c.*1100+50del	ENSP00000493608.1:n.*1100+50del
ENST00000644319.1:n.1708+50del
ENST00000645901.1:n.2184+50del
ENST00000646391.1:c.*1103+50del	ENSP00000494104.1:n.*1103+50del
ENST00000646625.1:c.1333+50del	ENSP00000496263.1:n.1333+50del
ENST00000647279.1:c.*572+50del	ENSP00000494502.1:n.*572+50del
ENST00000647506.1:n.2209+50del
ENST00000647534.1:n.397+50del
ENST00000298552.7:c.1333+50del	ENSP00000298552.3:n.1333+50del
ENST00000440111.6:c.1333+50del	ENSP00000394524.2:n.1333+50del
ENST00000545250.5:c.1180+50del	ENSP00000444017.1:n.1180+50del
NM_000368.4:c.1333+50del , LRG_486t1:c.1333+50del	NP_000359.1:n.1333+50del
NM_001162426.1:c.1330+50del	NP_001155898.1:n.1330+50del
NM_001162427.1:c.1180+50del	NP_001155899.1:n.1180+50del
XM_005272211.1:c.1333+50del	XP_005272268.1:n.1333+50del
XM_006717271.1:c.1333+50del	XP_006717334.1:n.1333+50del
XM_006717272.2:c.1333+50del	XP_006717335.1:n.1333+50del
XM_011518979.1:c.1333+50del	XP_011517281.1:n.1333+50del
NM_001362177.1:c.970+50del	NP_001349106.1:n.970+50del
XM_011518979.2:c.1333+50del	XP_011517281.1:n.1333+50del
XM_017015096.1:c.1333+50del	XP_016870585.1:n.1333+50del
XM_017015097.1:c.1333+50del	XP_016870586.1:n.1333+50del
XM_017015098.1:c.1330+50del	XP_016870587.1:n.1330+50del
XM_017015100.1:c.970+50del	XP_016870589.1:n.970+50del
XM_017015101.1:c.967+50del	XP_016870590.1:n.967+50del
NM_000368.5:c.1333+50del MANE Select	NP_000359.1:n.1333+50del
NM_001162426.2:c.1330+50del	NP_001155898.1:n.1330+50del
NM_001162427.2:c.1180+50del	NP_001155899.1:n.1180+50del
NM_001362177.2:c.970+50del	NP_001349106.1:n.970+50del