Canonical Allele Identifier: CA375367614

Gene: TSC1

Linked Data

• ClinVar Variation Id: 466116
• ClinVar RCV Id: RCV000531464 ; RCV003352915
• dbSNP Id: rs1554812917
• gnomAD v4: 9-132896662-G-A
• MyVariant Identifiers: chr9:g.135772049G>A (hg19) ; chr9:g.132896662G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132896662G>A , CM000671.2:g.132896662G>A	GRCh38
NC_000009.11:g.135772049G>A , CM000671.1:g.135772049G>A	GRCh37
NC_000009.10:g.134761870G>A	NCBI36
NG_012386.1:g.52972C>T , LRG_486:g.52972C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475903.7:c.3065C>T	ENSP00000496126.2:p.Pro1022Leu
ENST00000490179.4:c.3068C>T	ENSP00000495533.2:p.Pro1023Leu
ENST00000642261.2:c.*924C>T	ENSP00000494743.2:n.*924C>T
ENST00000643275.2:c.*1008C>T	ENSP00000495598.2:n.*1008C>T
ENST00000643362.2:c.2681C>T	ENSP00000496398.2:p.Pro894Leu
ENST00000643625.2:c.*810C>T	ENSP00000495546.2:n.*810C>T
ENST00000643691.2:c.2705C>T	ENSP00000494916.2:p.Pro902Leu
ENST00000644184.2:c.3026C>T	ENSP00000495428.2:p.Pro1009Leu
ENST00000645129.2:c.2912C>T	ENSP00000493639.2:p.Pro971Leu
ENST00000646440.2:c.3068C>T	ENSP00000495830.2:p.Pro1023Leu
ENST00000298552.9:c.3068C>T MANE Select	ENSP00000298552.3:p.Pro1023Leu
ENST00000642261.1:c.1205C>T
ENST00000642617.1:c.3065C>T	ENSP00000493773.1:p.Pro1022Leu
ENST00000642627.1:c.3050C>T	ENSP00000496772.1:p.Pro1017Leu
ENST00000642811.1:c.*2838C>T	ENSP00000495554.1:n.*2838C>T
ENST00000643072.1:c.2915C>T	ENSP00000496691.1:p.Pro972Leu
ENST00000643275.1:c.1542C>T	ENSP00000495598.1:n.1542C>T
ENST00000643583.1:c.3053C>T	ENSP00000494685.1:p.Pro1018Leu
ENST00000643625.1:c.945C>T	ENSP00000495546.1:n.945C>T
ENST00000643875.1:c.3068C>T	ENSP00000495158.1:p.Pro1023Leu
ENST00000644097.1:c.3065C>T	ENSP00000494682.1:p.Pro1022Leu
ENST00000644184.1:c.1763C>T	ENSP00000495428.1:p.Pro588Leu
ENST00000644255.1:c.*2835C>T	ENSP00000493608.1:n.*2835C>T
ENST00000644319.1:n.3443C>T
ENST00000644786.1:n.727C>T
ENST00000644882.1:n.1976C>T
ENST00000645901.1:n.3919C>T
ENST00000646391.1:c.*2838C>T	ENSP00000494104.1:n.*2838C>T
ENST00000646625.1:c.3068C>T	ENSP00000496263.1:p.Pro1023Leu
ENST00000647262.1:n.2033C>T
ENST00000647279.1:c.*2307C>T	ENSP00000494502.1:n.*2307C>T
ENST00000647534.1:n.2132C>T
ENST00000298552.7:c.3068C>T	ENSP00000298552.3:p.Pro1023Leu
ENST00000440111.6:c.3068C>T	ENSP00000394524.2:p.Pro1023Leu
ENST00000545250.5:c.2915C>T	ENSP00000444017.1:p.Pro972Leu
NM_000368.4:c.3068C>T , LRG_486t1:c.3068C>T	NP_000359.1:p.Pro1023Leu
NM_001162426.1:c.3065C>T	NP_001155898.1:p.Pro1022Leu
NM_001162427.1:c.2915C>T	NP_001155899.1:p.Pro972Leu
XM_005272211.1:c.3068C>T	XP_005272268.1:p.Pro1023Leu
XM_006717271.1:c.3068C>T	XP_006717334.1:p.Pro1023Leu
XM_011518979.1:c.3068C>T	XP_011517281.1:p.Pro1023Leu
NM_001362177.1:c.2705C>T	NP_001349106.1:p.Pro902Leu
XM_011518979.2:c.3068C>T	XP_011517281.1:p.Pro1023Leu
XM_017015096.1:c.3068C>T	XP_016870585.1:p.Pro1023Leu
XM_017015097.1:c.3068C>T	XP_016870586.1:p.Pro1023Leu
XM_017015098.1:c.3065C>T	XP_016870587.1:p.Pro1022Leu
XM_017015100.1:c.2705C>T	XP_016870589.1:p.Pro902Leu
XM_017015101.1:c.2702C>T	XP_016870590.1:p.Pro901Leu
NM_000368.5:c.3068C>T MANE Select	NP_000359.1:p.Pro1023Leu
NM_001162426.2:c.3065C>T	NP_001155898.1:p.Pro1022Leu
NM_001162427.2:c.2915C>T	NP_001155899.1:p.Pro972Leu
NM_001362177.2:c.2705C>T	NP_001349106.1:p.Pro902Leu