Canonical Allele Identifier: CA375366493

Gene: TSC1

Linked Data

• ClinVar Variation Id: 1497174
• ClinVar RCV Id: RCV001992257 ; RCV002458957
• dbSNP Id: rs1845037495
• gnomAD v4: 9-132896351-C-A
• MyVariant Identifiers: chr9:g.135771738C>A (hg19) ; chr9:g.132896351C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132896351C>A , CM000671.2:g.132896351C>A	GRCh38
NC_000009.11:g.135771738C>A , CM000671.1:g.135771738C>A	GRCh37
NC_000009.10:g.134761559C>A	NCBI36
NG_012386.1:g.53283G>T , LRG_486:g.53283G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000475903.7:c.3376G>T	ENSP00000496126.2:p.Val1126Leu
ENST00000490179.4:c.3379G>T	ENSP00000495533.2:p.Val1127Leu
ENST00000642261.2:c.*1235G>T	ENSP00000494743.2:n.*1235G>T
ENST00000643275.2:c.*1319G>T	ENSP00000495598.2:n.*1319G>T
ENST00000643362.2:c.2992G>T	ENSP00000496398.2:p.Val998Leu
ENST00000643625.2:c.*1121G>T	ENSP00000495546.2:n.*1121G>T
ENST00000643691.2:c.3016G>T	ENSP00000494916.2:p.Val1006Leu
ENST00000644184.2:c.3337G>T	ENSP00000495428.2:p.Val1113Leu
ENST00000645129.2:c.3223G>T	ENSP00000493639.2:p.Val1075Leu
ENST00000646440.2:c.3379G>T	ENSP00000495830.2:p.Val1127Leu
ENST00000298552.9:c.3379G>T MANE Select	ENSP00000298552.3:p.Val1127Leu
ENST00000642617.1:c.3376G>T	ENSP00000493773.1:p.Val1126Leu
ENST00000642627.1:c.3361G>T	ENSP00000496772.1:p.Val1121Leu
ENST00000642811.1:c.*3149G>T	ENSP00000495554.1:n.*3149G>T
ENST00000643072.1:c.3226G>T	ENSP00000496691.1:p.Val1076Leu
ENST00000643583.1:c.3364G>T	ENSP00000494685.1:p.Val1122Leu
ENST00000643625.1:c.1256G>T	ENSP00000495546.1:n.1256G>T
ENST00000643875.1:c.3379G>T	ENSP00000495158.1:p.Val1127Leu
ENST00000644097.1:c.3376G>T	ENSP00000494682.1:p.Val1126Leu
ENST00000644184.1:c.2074G>T	ENSP00000495428.1:p.Val692Leu
ENST00000644255.1:c.*3146G>T	ENSP00000493608.1:n.*3146G>T
ENST00000644319.1:n.3754G>T
ENST00000644786.1:n.1038G>T
ENST00000644882.1:n.2287G>T
ENST00000645901.1:n.4230G>T
ENST00000646391.1:c.*3149G>T	ENSP00000494104.1:n.*3149G>T
ENST00000646625.1:c.3379G>T	ENSP00000496263.1:p.Val1127Leu
ENST00000647262.1:n.2344G>T
ENST00000647279.1:c.*2618G>T	ENSP00000494502.1:n.*2618G>T
ENST00000647534.1:n.2443G>T
ENST00000298552.7:c.3379G>T	ENSP00000298552.3:p.Val1127Leu
ENST00000440111.6:c.3379G>T	ENSP00000394524.2:p.Val1127Leu
ENST00000545250.5:c.3226G>T	ENSP00000444017.1:p.Val1076Leu
NM_000368.4:c.3379G>T , LRG_486t1:c.3379G>T	NP_000359.1:p.Val1127Leu
NM_001162426.1:c.3376G>T	NP_001155898.1:p.Val1126Leu
NM_001162427.1:c.3226G>T	NP_001155899.1:p.Val1076Leu
XM_005272211.1:c.3379G>T	XP_005272268.1:p.Val1127Leu
XM_006717271.1:c.3379G>T	XP_006717334.1:p.Val1127Leu
XM_011518979.1:c.3379G>T	XP_011517281.1:p.Val1127Leu
NM_001362177.1:c.3016G>T	NP_001349106.1:p.Val1006Leu
XM_011518979.2:c.3379G>T	XP_011517281.1:p.Val1127Leu
XM_017015096.1:c.3379G>T	XP_016870585.1:p.Val1127Leu
XM_017015097.1:c.3379G>T	XP_016870586.1:p.Val1127Leu
XM_017015098.1:c.3376G>T	XP_016870587.1:p.Val1126Leu
XM_017015100.1:c.3016G>T	XP_016870589.1:p.Val1006Leu
XM_017015101.1:c.3013G>T	XP_016870590.1:p.Val1005Leu
NM_000368.5:c.3379G>T MANE Select	NP_000359.1:p.Val1127Leu
NM_001162426.2:c.3376G>T	NP_001155898.1:p.Val1126Leu
NM_001162427.2:c.3226G>T	NP_001155899.1:p.Val1076Leu
NM_001362177.2:c.3016G>T	NP_001349106.1:p.Val1006Leu