Canonical Allele Identifier: CA467812850

Gene: TSC1

Linked Data

• ClinVar Variation Id: 2026304
• ClinVar RCV Id: RCV002889193
• gnomAD v4: 9-132896259-A-G
• MyVariant Identifiers: chr9:g.135771646A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132896259A>G , CM000671.2:g.132896259A>G	GRCh38
NC_000009.11:g.135771646A>G , CM000671.1:g.135771646A>G	GRCh37
NC_000009.10:g.134761467A>G	NCBI36
NG_012386.1:g.53375T>C , LRG_486:g.53375T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475903.7:c.3468T>C	ENSP00000496126.2:p.Asn1156=
ENST00000490179.4:c.3471T>C	ENSP00000495533.2:p.Asn1157=
ENST00000642261.2:c.*1327T>C	ENSP00000494743.2:n.*1327T>C
ENST00000643275.2:c.*1411T>C	ENSP00000495598.2:n.*1411T>C
ENST00000643362.2:c.3084T>C	ENSP00000496398.2:p.Asn1028=
ENST00000643625.2:c.*1213T>C	ENSP00000495546.2:n.*1213T>C
ENST00000643691.2:c.3108T>C	ENSP00000494916.2:p.Asn1036=
ENST00000644184.2:c.3429T>C	ENSP00000495428.2:p.Asn1143=
ENST00000645129.2:c.3315T>C	ENSP00000493639.2:p.Asn1105=
ENST00000646440.2:c.3471T>C	ENSP00000495830.2:p.Asn1157=
ENST00000298552.9:c.3471T>C MANE Select	ENSP00000298552.3:p.Asn1157=
ENST00000642617.1:c.3468T>C	ENSP00000493773.1:p.Asn1156=
ENST00000642627.1:c.3453T>C	ENSP00000496772.1:p.Asn1151=
ENST00000642811.1:c.*3241T>C	ENSP00000495554.1:n.*3241T>C
ENST00000643072.1:c.3318T>C	ENSP00000496691.1:p.Asn1106=
ENST00000643583.1:c.3456T>C	ENSP00000494685.1:p.Asn1152=
ENST00000643625.1:c.1348T>C	ENSP00000495546.1:n.1348T>C
ENST00000643875.1:c.3471T>C	ENSP00000495158.1:p.Asn1157=
ENST00000644097.1:c.3468T>C	ENSP00000494682.1:p.Asn1156=
ENST00000644184.1:c.2166T>C	ENSP00000495428.1:p.Asn722=
ENST00000644255.1:c.*3238T>C	ENSP00000493608.1:n.*3238T>C
ENST00000644319.1:n.3846T>C
ENST00000644786.1:n.1130T>C
ENST00000644882.1:n.2379T>C
ENST00000645901.1:n.4322T>C
ENST00000646391.1:c.*3241T>C	ENSP00000494104.1:n.*3241T>C
ENST00000646625.1:c.3471T>C	ENSP00000496263.1:p.Asn1157=
ENST00000647262.1:n.2436T>C
ENST00000647279.1:c.*2710T>C	ENSP00000494502.1:n.*2710T>C
ENST00000647534.1:n.2535T>C
ENST00000298552.7:c.3471T>C	ENSP00000298552.3:p.Asn1157=
ENST00000440111.6:c.3471T>C	ENSP00000394524.2:p.Asn1157=
ENST00000545250.5:c.3318T>C	ENSP00000444017.1:p.Asn1106=
NM_000368.4:c.3471T>C , LRG_486t1:c.3471T>C	NP_000359.1:p.Asn1157=
NM_001162426.1:c.3468T>C	NP_001155898.1:p.Asn1156=
NM_001162427.1:c.3318T>C	NP_001155899.1:p.Asn1106=
XM_005272211.1:c.3471T>C	XP_005272268.1:p.Asn1157=
XM_006717271.1:c.3471T>C	XP_006717334.1:p.Asn1157=
XM_011518979.1:c.3471T>C	XP_011517281.1:p.Asn1157=
NM_001362177.1:c.3108T>C	NP_001349106.1:p.Asn1036=
XM_011518979.2:c.3471T>C	XP_011517281.1:p.Asn1157=
XM_017015096.1:c.3471T>C	XP_016870585.1:p.Asn1157=
XM_017015097.1:c.3471T>C	XP_016870586.1:p.Asn1157=
XM_017015098.1:c.3468T>C	XP_016870587.1:p.Asn1156=
XM_017015100.1:c.3108T>C	XP_016870589.1:p.Asn1036=
XM_017015101.1:c.3105T>C	XP_016870590.1:p.Asn1035=
NM_000368.5:c.3471T>C MANE Select	NP_000359.1:p.Asn1157=
NM_001162426.2:c.3468T>C	NP_001155898.1:p.Asn1156=
NM_001162427.2:c.3318T>C	NP_001155899.1:p.Asn1106=
NM_001362177.2:c.3108T>C	NP_001349106.1:p.Asn1036=