Canonical Allele Identifier: CA2692286578

Gene: TSC1

Linked Data

• gnomAD v4: 9-132903637-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132903641del , CM000671.2:g.132903641del	GRCh38
NC_000009.11:g.135779028del , CM000671.1:g.135779028del	GRCh37
NC_000009.10:g.134768849del	NCBI36
NG_012386.1:g.45996del , LRG_486:g.45996del

Transcript Alleles

HGVS	Amino-acid change
ENST00000475903.7:c.2205+13del	ENSP00000496126.2:n.2205+13del
ENST00000490179.4:c.2208+13del	ENSP00000495533.2:n.2208+13del
ENST00000642261.2:c.2208+13del	ENSP00000494743.2:n.2208+13del
ENST00000643275.2:c.*148+13del	ENSP00000495598.2:n.*148+13del
ENST00000643362.2:c.1821+13del	ENSP00000496398.2:n.1821+13del
ENST00000643625.2:c.2041+773del	ENSP00000495546.2:n.2041+773del
ENST00000643691.2:c.1845+13del	ENSP00000494916.2:n.1845+13del
ENST00000644184.2:c.2208+13del	ENSP00000495428.2:n.2208+13del
ENST00000645129.2:c.2052+13del	ENSP00000493639.2:n.2052+13del
ENST00000646440.2:c.2208+13del	ENSP00000495830.2:n.2208+13del
ENST00000298552.9:c.2208+13del MANE Select	ENSP00000298552.3:n.2208+13del
ENST00000642261.1:c.272+13del
ENST00000642617.1:c.2205+13del	ENSP00000493773.1:n.2205+13del
ENST00000642627.1:c.2190+13del	ENSP00000496772.1:n.2190+13del
ENST00000642811.1:c.*1978+13del	ENSP00000495554.1:n.*1978+13del
ENST00000643072.1:c.2055+13del	ENSP00000496691.1:n.2055+13del
ENST00000643275.1:c.682+13del	ENSP00000495598.1:n.682+13del
ENST00000643583.1:c.2193+13del	ENSP00000494685.1:n.2193+13del
ENST00000643625.1:c.85+773del	ENSP00000495546.1:n.85+773del
ENST00000643875.1:c.2208+13del	ENSP00000495158.1:n.2208+13del
ENST00000644097.1:c.2205+13del	ENSP00000494682.1:n.2205+13del
ENST00000644184.1:c.945+13del	ENSP00000495428.1:n.945+13del
ENST00000644255.1:c.*1975+13del	ENSP00000493608.1:n.*1975+13del
ENST00000644319.1:n.2583+13del
ENST00000644882.1:n.1163+13del
ENST00000645901.1:n.3059+13del
ENST00000646391.1:c.*1978+13del	ENSP00000494104.1:n.*1978+13del
ENST00000646625.1:c.2208+13del	ENSP00000496263.1:n.2208+13del
ENST00000647262.1:n.1173+13del
ENST00000647279.1:c.*1447+13del	ENSP00000494502.1:n.*1447+13del
ENST00000647506.1:n.3084+13del
ENST00000647534.1:n.1272+13del
ENST00000298552.7:c.2208+13del	ENSP00000298552.3:n.2208+13del
ENST00000440111.6:c.2208+13del	ENSP00000394524.2:n.2208+13del
ENST00000545250.5:c.2055+13del	ENSP00000444017.1:n.2055+13del
NM_000368.4:c.2208+13del , LRG_486t1:c.2208+13del	NP_000359.1:n.2208+13del
NM_001162426.1:c.2205+13del	NP_001155898.1:n.2205+13del
NM_001162427.1:c.2055+13del	NP_001155899.1:n.2055+13del
XM_005272211.1:c.2208+13del	XP_005272268.1:n.2208+13del
XM_006717271.1:c.2208+13del	XP_006717334.1:n.2208+13del
XM_011518979.1:c.2208+13del	XP_011517281.1:n.2208+13del
NM_001362177.1:c.1845+13del	NP_001349106.1:n.1845+13del
XM_011518979.2:c.2208+13del	XP_011517281.1:n.2208+13del
XM_017015096.1:c.2208+13del	XP_016870585.1:n.2208+13del
XM_017015097.1:c.2208+13del	XP_016870586.1:n.2208+13del
XM_017015098.1:c.2205+13del	XP_016870587.1:n.2205+13del
XM_017015100.1:c.1845+13del	XP_016870589.1:n.1845+13del
XM_017015101.1:c.1842+13del	XP_016870590.1:n.1842+13del
NM_000368.5:c.2208+13del MANE Select	NP_000359.1:n.2208+13del
NM_001162426.2:c.2205+13del	NP_001155898.1:n.2205+13del
NM_001162427.2:c.2055+13del	NP_001155899.1:n.2055+13del
NM_001362177.2:c.1845+13del	NP_001349106.1:n.1845+13del