Canonical Allele Identifier: CA006014

Gene: TSC1

Linked Data

• ClinVar Variation Id: 48896
• ClinVar RCV Id: RCV000042147
• dbSNP Id: rs118203639
• MyVariant Identifiers: chr9:g.135779143C>A (hg19) ; chr9:g.132903756C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132903756C>A , CM000671.2:g.132903756C>A	GRCh38
NC_000009.11:g.135779143C>A , CM000671.1:g.135779143C>A	GRCh37
NC_000009.10:g.134768964C>A	NCBI36
NG_012386.1:g.45878G>T , LRG_486:g.45878G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475903.7:c.2100G>T	ENSP00000496126.2:p.Gln700His
ENST00000490179.4:c.2103G>T	ENSP00000495533.2:p.Gln701His
ENST00000642261.2:c.2103G>T	ENSP00000494743.2:p.Gln701His
ENST00000643275.2:c.*43G>T	ENSP00000495598.2:n.*43G>T
ENST00000643362.2:c.1716G>T	ENSP00000496398.2:p.Gln572His
ENST00000643625.2:c.2041+655G>T	ENSP00000495546.2:n.2041+655G>T
ENST00000643691.2:c.1740G>T	ENSP00000494916.2:p.Gln580His
ENST00000644184.2:c.2103G>T	ENSP00000495428.2:p.Gln701His
ENST00000645129.2:c.1947G>T	ENSP00000493639.2:p.Gln649His
ENST00000646440.2:c.2103G>T	ENSP00000495830.2:p.Gln701His
ENST00000298552.9:c.2103G>T MANE Select	ENSP00000298552.3:p.Gln701His
ENST00000642261.1:c.167G>T
ENST00000642617.1:c.2100G>T	ENSP00000493773.1:p.Gln700His
ENST00000642627.1:c.2085G>T	ENSP00000496772.1:p.Gln695His
ENST00000642811.1:c.*1873G>T	ENSP00000495554.1:n.*1873G>T
ENST00000643072.1:c.1950G>T	ENSP00000496691.1:p.Gln650His
ENST00000643275.1:c.577G>T	ENSP00000495598.1:n.577G>T
ENST00000643583.1:c.2088G>T	ENSP00000494685.1:p.Gln696His
ENST00000643625.1:c.85+655G>T	ENSP00000495546.1:n.85+655G>T
ENST00000643875.1:c.2103G>T	ENSP00000495158.1:p.Gln701His
ENST00000644097.1:c.2100G>T	ENSP00000494682.1:p.Gln700His
ENST00000644184.1:c.840G>T	ENSP00000495428.1:p.Gln280His
ENST00000644255.1:c.*1870G>T	ENSP00000493608.1:n.*1870G>T
ENST00000644319.1:n.2478G>T
ENST00000644882.1:n.1058G>T
ENST00000645901.1:n.2954G>T
ENST00000646391.1:c.*1873G>T	ENSP00000494104.1:n.*1873G>T
ENST00000646625.1:c.2103G>T	ENSP00000496263.1:p.Gln701His
ENST00000647262.1:n.1068G>T
ENST00000647279.1:c.*1342G>T	ENSP00000494502.1:n.*1342G>T
ENST00000647506.1:n.2979G>T
ENST00000647534.1:n.1167G>T
ENST00000298552.7:c.2103G>T	ENSP00000298552.3:p.Gln701His
ENST00000440111.6:c.2103G>T	ENSP00000394524.2:p.Gln701His
ENST00000545250.5:c.1950G>T	ENSP00000444017.1:p.Gln650His
NM_000368.4:c.2103G>T , LRG_486t1:c.2103G>T	NP_000359.1:p.Gln701His
NM_001162426.1:c.2100G>T	NP_001155898.1:p.Gln700His
NM_001162427.1:c.1950G>T	NP_001155899.1:p.Gln650His
XM_005272211.1:c.2103G>T	XP_005272268.1:p.Gln701His
XM_006717271.1:c.2103G>T	XP_006717334.1:p.Gln701His
XM_011518979.1:c.2103G>T	XP_011517281.1:p.Gln701His
NM_001362177.1:c.1740G>T	NP_001349106.1:p.Gln580His
XM_011518979.2:c.2103G>T	XP_011517281.1:p.Gln701His
XM_017015096.1:c.2103G>T	XP_016870585.1:p.Gln701His
XM_017015097.1:c.2103G>T	XP_016870586.1:p.Gln701His
XM_017015098.1:c.2100G>T	XP_016870587.1:p.Gln700His
XM_017015100.1:c.1740G>T	XP_016870589.1:p.Gln580His
XM_017015101.1:c.1737G>T	XP_016870590.1:p.Gln579His
NM_000368.5:c.2103G>T MANE Select	NP_000359.1:p.Gln701His
NM_001162426.2:c.2100G>T	NP_001155898.1:p.Gln700His
NM_001162427.2:c.1950G>T	NP_001155899.1:p.Gln650His
NM_001362177.2:c.1740G>T	NP_001349106.1:p.Gln580His