Canonical Allele Identifier: CA375368691

Gene: TSC1

Linked Data

• dbSNP Id: rs2131979827
• MyVariant Identifiers: chr9:g.135786916A>G (hg19) ; chr9:g.132911529A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132911529A>G , CM000671.2:g.132911529A>G	GRCh38
NC_000009.11:g.135786916A>G , CM000671.1:g.135786916A>G	GRCh37
NC_000009.10:g.134776737A>G	NCBI36
NG_012386.1:g.38105T>C , LRG_486:g.38105T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475903.7:c.953T>C	ENSP00000496126.2:p.Met318Thr
ENST00000490179.4:c.953T>C	ENSP00000495533.2:p.Met318Thr
ENST00000642261.2:c.953T>C	ENSP00000494743.2:p.Met318Thr
ENST00000643275.2:c.953T>C	ENSP00000495598.2:p.Met318Thr
ENST00000643362.2:c.800T>C	ENSP00000496398.2:p.Met267Thr
ENST00000643625.2:c.953T>C	ENSP00000495546.2:p.Met318Thr
ENST00000643691.2:c.590T>C	ENSP00000494916.2:p.Met197Thr
ENST00000644184.2:c.953T>C	ENSP00000495428.2:p.Met318Thr
ENST00000645129.2:c.800T>C	ENSP00000493639.2:p.Met267Thr
ENST00000646440.2:c.953T>C	ENSP00000495830.2:p.Met318Thr
ENST00000647078.2:c.953T>C	ENSP00000496066.1:p.Met318Thr
ENST00000298552.9:c.953T>C MANE Select	ENSP00000298552.3:p.Met318Thr
ENST00000403810.6:c.953T>C	ENSP00000386093.1:p.Met318Thr
ENST00000493467.6:n.227T>C
ENST00000642344.1:c.*694T>C	ENSP00000494847.1:n.*694T>C
ENST00000642617.1:c.953T>C	ENSP00000493773.1:p.Met318Thr
ENST00000642627.1:c.953T>C	ENSP00000496772.1:p.Met318Thr
ENST00000642646.1:c.953T>C	ENSP00000496292.1:p.Met318Thr
ENST00000642745.1:c.953T>C	ENSP00000493963.1:p.Met318Thr
ENST00000642811.1:c.*723T>C	ENSP00000495554.1:n.*723T>C
ENST00000642854.1:c.*738T>C	ENSP00000494639.1:n.*738T>C
ENST00000643072.1:c.800T>C	ENSP00000496691.1:p.Met267Thr
ENST00000643362.1:c.800T>C	ENSP00000496398.1:p.Met267Thr
ENST00000643583.1:c.953T>C	ENSP00000494685.1:p.Met318Thr
ENST00000643691.1:c.590T>C	ENSP00000494916.1:p.Met197Thr
ENST00000643875.1:c.953T>C	ENSP00000495158.1:p.Met318Thr
ENST00000644097.1:c.953T>C	ENSP00000494682.1:p.Met318Thr
ENST00000644255.1:c.*723T>C	ENSP00000493608.1:n.*723T>C
ENST00000644319.1:n.680T>C
ENST00000644997.1:c.*610T>C	ENSP00000495654.1:n.*610T>C
ENST00000645129.1:c.800T>C	ENSP00000493639.1:p.Met267Thr
ENST00000645150.1:c.953T>C	ENSP00000494365.1:p.Met318Thr
ENST00000645901.1:n.1156T>C
ENST00000646391.1:c.*723T>C	ENSP00000494104.1:n.*723T>C
ENST00000646625.1:c.953T>C	ENSP00000496263.1:p.Met318Thr
ENST00000647078.1:c.953T>C	ENSP00000496066.1:p.Met318Thr
ENST00000647279.1:c.*192T>C	ENSP00000494502.1:n.*192T>C
ENST00000647462.1:c.953T>C	ENSP00000495821.1:p.Met318Thr
ENST00000647506.1:n.1181T>C
ENST00000298552.7:c.953T>C	ENSP00000298552.3:p.Met318Thr
ENST00000403810.5:c.953T>C	ENSP00000386093.1:p.Met318Thr
ENST00000440111.6:c.953T>C	ENSP00000394524.2:p.Met318Thr
ENST00000493467.5:n.1149T>C
ENST00000545250.5:c.800T>C	ENSP00000444017.1:p.Met267Thr
NM_000368.4:c.953T>C , LRG_486t1:c.953T>C	NP_000359.1:p.Met318Thr
NM_001162426.1:c.953T>C	NP_001155898.1:p.Met318Thr
NM_001162427.1:c.800T>C	NP_001155899.1:p.Met267Thr
XM_005272211.1:c.953T>C	XP_005272268.1:p.Met318Thr
XM_006717271.1:c.953T>C	XP_006717334.1:p.Met318Thr
XM_006717272.2:c.953T>C	XP_006717335.1:p.Met318Thr
XM_011518979.1:c.953T>C	XP_011517281.1:p.Met318Thr
NM_001362177.1:c.590T>C	NP_001349106.1:p.Met197Thr
XM_011518979.2:c.953T>C	XP_011517281.1:p.Met318Thr
XM_017015096.1:c.953T>C	XP_016870585.1:p.Met318Thr
XM_017015097.1:c.953T>C	XP_016870586.1:p.Met318Thr
XM_017015098.1:c.953T>C	XP_016870587.1:p.Met318Thr
XM_017015100.1:c.590T>C	XP_016870589.1:p.Met197Thr
XM_017015101.1:c.590T>C	XP_016870590.1:p.Met197Thr
NM_000368.5:c.953T>C MANE Select	NP_000359.1:p.Met318Thr
NM_001162426.2:c.953T>C	NP_001155898.1:p.Met318Thr
NM_001162427.2:c.800T>C	NP_001155899.1:p.Met267Thr
NM_001362177.2:c.590T>C	NP_001349106.1:p.Met197Thr