Canonical Allele Identifier: CA375366324

Gene: TSC1

Linked Data

• MyVariant Identifiers: chr9:g.135771655C>G (hg19) ; chr9:g.132896268C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132896268C>G , CM000671.2:g.132896268C>G	GRCh38
NC_000009.11:g.135771655C>G , CM000671.1:g.135771655C>G	GRCh37
NC_000009.10:g.134761476C>G	NCBI36
NG_012386.1:g.53366G>C , LRG_486:g.53366G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475903.7:c.3459G>C	ENSP00000496126.2:p.Met1153Ile
ENST00000490179.4:c.3462G>C	ENSP00000495533.2:p.Met1154Ile
ENST00000642261.2:c.*1318G>C	ENSP00000494743.2:n.*1318G>C
ENST00000643275.2:c.*1402G>C	ENSP00000495598.2:n.*1402G>C
ENST00000643362.2:c.3075G>C	ENSP00000496398.2:p.Met1025Ile
ENST00000643625.2:c.*1204G>C	ENSP00000495546.2:n.*1204G>C
ENST00000643691.2:c.3099G>C	ENSP00000494916.2:p.Met1033Ile
ENST00000644184.2:c.3420G>C	ENSP00000495428.2:p.Met1140Ile
ENST00000645129.2:c.3306G>C	ENSP00000493639.2:p.Met1102Ile
ENST00000646440.2:c.3462G>C	ENSP00000495830.2:p.Met1154Ile
ENST00000298552.9:c.3462G>C MANE Select	ENSP00000298552.3:p.Met1154Ile
ENST00000642617.1:c.3459G>C	ENSP00000493773.1:p.Met1153Ile
ENST00000642627.1:c.3444G>C	ENSP00000496772.1:p.Met1148Ile
ENST00000642811.1:c.*3232G>C	ENSP00000495554.1:n.*3232G>C
ENST00000643072.1:c.3309G>C	ENSP00000496691.1:p.Met1103Ile
ENST00000643583.1:c.3447G>C	ENSP00000494685.1:p.Met1149Ile
ENST00000643625.1:c.1339G>C	ENSP00000495546.1:n.1339G>C
ENST00000643875.1:c.3462G>C	ENSP00000495158.1:p.Met1154Ile
ENST00000644097.1:c.3459G>C	ENSP00000494682.1:p.Met1153Ile
ENST00000644184.1:c.2157G>C	ENSP00000495428.1:p.Met719Ile
ENST00000644255.1:c.*3229G>C	ENSP00000493608.1:n.*3229G>C
ENST00000644319.1:n.3837G>C
ENST00000644786.1:n.1121G>C
ENST00000644882.1:n.2370G>C
ENST00000645901.1:n.4313G>C
ENST00000646391.1:c.*3232G>C	ENSP00000494104.1:n.*3232G>C
ENST00000646625.1:c.3462G>C	ENSP00000496263.1:p.Met1154Ile
ENST00000647262.1:n.2427G>C
ENST00000647279.1:c.*2701G>C	ENSP00000494502.1:n.*2701G>C
ENST00000647534.1:n.2526G>C
ENST00000298552.7:c.3462G>C	ENSP00000298552.3:p.Met1154Ile
ENST00000440111.6:c.3462G>C	ENSP00000394524.2:p.Met1154Ile
ENST00000545250.5:c.3309G>C	ENSP00000444017.1:p.Met1103Ile
NM_000368.4:c.3462G>C , LRG_486t1:c.3462G>C	NP_000359.1:p.Met1154Ile
NM_001162426.1:c.3459G>C	NP_001155898.1:p.Met1153Ile
NM_001162427.1:c.3309G>C	NP_001155899.1:p.Met1103Ile
XM_005272211.1:c.3462G>C	XP_005272268.1:p.Met1154Ile
XM_006717271.1:c.3462G>C	XP_006717334.1:p.Met1154Ile
XM_011518979.1:c.3462G>C	XP_011517281.1:p.Met1154Ile
NM_001362177.1:c.3099G>C	NP_001349106.1:p.Met1033Ile
XM_011518979.2:c.3462G>C	XP_011517281.1:p.Met1154Ile
XM_017015096.1:c.3462G>C	XP_016870585.1:p.Met1154Ile
XM_017015097.1:c.3462G>C	XP_016870586.1:p.Met1154Ile
XM_017015098.1:c.3459G>C	XP_016870587.1:p.Met1153Ile
XM_017015100.1:c.3099G>C	XP_016870589.1:p.Met1033Ile
XM_017015101.1:c.3096G>C	XP_016870590.1:p.Met1032Ile
NM_000368.5:c.3462G>C MANE Select	NP_000359.1:p.Met1154Ile
NM_001162426.2:c.3459G>C	NP_001155898.1:p.Met1153Ile
NM_001162427.2:c.3309G>C	NP_001155899.1:p.Met1103Ile
NM_001362177.2:c.3099G>C	NP_001349106.1:p.Met1033Ile