Canonical Allele Identifier: CA375369819

Gene: TSC1

Linked Data

• ClinVar Variation Id: 1695272
• ClinVar RCV Id: RCV002263522
• dbSNP Id: rs777437357
• MyVariant Identifiers: chr9:g.135776102C>G (hg19) ; chr9:g.132900715C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132900715C>G , CM000671.2:g.132900715C>G	GRCh38
NC_000009.11:g.135776102C>G , CM000671.1:g.135776102C>G	GRCh37
NC_000009.10:g.134765923C>G	NCBI36
NG_012386.1:g.48919G>C , LRG_486:g.48919G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000475903.7:c.2622G>C	ENSP00000496126.2:p.Lys874Asn
ENST00000490179.4:c.2625G>C	ENSP00000495533.2:p.Lys875Asn
ENST00000642261.2:c.*404G>C	ENSP00000494743.2:n.*404G>C
ENST00000643275.2:c.*565G>C	ENSP00000495598.2:n.*565G>C
ENST00000643362.2:c.2238G>C	ENSP00000496398.2:p.Lys746Asn
ENST00000643625.2:c.*367G>C	ENSP00000495546.2:n.*367G>C
ENST00000643691.2:c.2262G>C	ENSP00000494916.2:p.Lys754Asn
ENST00000644184.2:c.2583G>C	ENSP00000495428.2:p.Lys861Asn
ENST00000645129.2:c.2469G>C	ENSP00000493639.2:p.Lys823Asn
ENST00000646440.2:c.2625G>C	ENSP00000495830.2:p.Lys875Asn
ENST00000298552.9:c.2625G>C MANE Select	ENSP00000298552.3:p.Lys875Asn
ENST00000642261.1:c.685G>C
ENST00000642617.1:c.2622G>C	ENSP00000493773.1:p.Lys874Asn
ENST00000642627.1:c.2607G>C	ENSP00000496772.1:p.Lys869Asn
ENST00000642811.1:c.*2395G>C	ENSP00000495554.1:n.*2395G>C
ENST00000643072.1:c.2472G>C	ENSP00000496691.1:p.Lys824Asn
ENST00000643275.1:c.1099G>C	ENSP00000495598.1:n.1099G>C
ENST00000643583.1:c.2610G>C	ENSP00000494685.1:p.Lys870Asn
ENST00000643625.1:c.502G>C	ENSP00000495546.1:n.502G>C
ENST00000643875.1:c.2625G>C	ENSP00000495158.1:p.Lys875Asn
ENST00000644097.1:c.2622G>C	ENSP00000494682.1:p.Lys874Asn
ENST00000644184.1:c.1320G>C	ENSP00000495428.1:p.Lys440Asn
ENST00000644255.1:c.*2392G>C	ENSP00000493608.1:n.*2392G>C
ENST00000644319.1:n.3000G>C
ENST00000644786.1:n.284G>C
ENST00000644882.1:n.1538G>C
ENST00000645901.1:n.3476G>C
ENST00000646391.1:c.*2395G>C	ENSP00000494104.1:n.*2395G>C
ENST00000646625.1:c.2625G>C	ENSP00000496263.1:p.Lys875Asn
ENST00000647262.1:n.1590G>C
ENST00000647279.1:c.*1864G>C	ENSP00000494502.1:n.*1864G>C
ENST00000647506.1:n.3501G>C
ENST00000647534.1:n.1689G>C
ENST00000298552.7:c.2625G>C	ENSP00000298552.3:p.Lys875Asn
ENST00000440111.6:c.2625G>C	ENSP00000394524.2:p.Lys875Asn
ENST00000545250.5:c.2472G>C	ENSP00000444017.1:p.Lys824Asn
NM_000368.4:c.2625G>C , LRG_486t1:c.2625G>C	NP_000359.1:p.Lys875Asn
NM_001162426.1:c.2622G>C	NP_001155898.1:p.Lys874Asn
NM_001162427.1:c.2472G>C	NP_001155899.1:p.Lys824Asn
XM_005272211.1:c.2625G>C	XP_005272268.1:p.Lys875Asn
XM_006717271.1:c.2625G>C	XP_006717334.1:p.Lys875Asn
XM_011518979.1:c.2625G>C	XP_011517281.1:p.Lys875Asn
NM_001362177.1:c.2262G>C	NP_001349106.1:p.Lys754Asn
XM_011518979.2:c.2625G>C	XP_011517281.1:p.Lys875Asn
XM_017015096.1:c.2625G>C	XP_016870585.1:p.Lys875Asn
XM_017015097.1:c.2625G>C	XP_016870586.1:p.Lys875Asn
XM_017015098.1:c.2622G>C	XP_016870587.1:p.Lys874Asn
XM_017015100.1:c.2262G>C	XP_016870589.1:p.Lys754Asn
XM_017015101.1:c.2259G>C	XP_016870590.1:p.Lys753Asn
NM_000368.5:c.2625G>C MANE Select	NP_000359.1:p.Lys875Asn
NM_001162426.2:c.2622G>C	NP_001155898.1:p.Lys874Asn
NM_001162427.2:c.2472G>C	NP_001155899.1:p.Lys824Asn
NM_001362177.2:c.2262G>C	NP_001349106.1:p.Lys754Asn