Canonical Allele Identifier: CA375366154

Gene: TSC1

Linked Data

• MyVariant Identifiers: chr9:g.135782723T>G (hg19) ; chr9:g.132907336T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132907336T>G , CM000671.2:g.132907336T>G	GRCh38
NC_000009.11:g.135782723T>G , CM000671.1:g.135782723T>G	GRCh37
NC_000009.10:g.134772544T>G	NCBI36
NG_012386.1:g.42298A>C , LRG_486:g.42298A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000475903.7:c.1295A>C	ENSP00000496126.2:p.His432Pro
ENST00000490179.4:c.1298A>C	ENSP00000495533.2:p.His433Pro
ENST00000642261.2:c.1298A>C	ENSP00000494743.2:p.His433Pro
ENST00000643275.2:c.1298A>C	ENSP00000495598.2:p.His433Pro
ENST00000643362.2:c.911A>C	ENSP00000496398.2:p.His304Pro
ENST00000643625.2:c.1298A>C	ENSP00000495546.2:p.His433Pro
ENST00000643691.2:c.935A>C	ENSP00000494916.2:p.His312Pro
ENST00000644184.2:c.1298A>C	ENSP00000495428.2:p.His433Pro
ENST00000645129.2:c.1142A>C	ENSP00000493639.2:p.His381Pro
ENST00000646440.2:c.1298A>C	ENSP00000495830.2:p.His433Pro
ENST00000298552.9:c.1298A>C MANE Select	ENSP00000298552.3:p.His433Pro
ENST00000642344.1:c.*1039A>C	ENSP00000494847.1:n.*1039A>C
ENST00000642617.1:c.1295A>C	ENSP00000493773.1:p.His432Pro
ENST00000642627.1:c.1295A>C	ENSP00000496772.1:p.His432Pro
ENST00000642811.1:c.*1068A>C	ENSP00000495554.1:n.*1068A>C
ENST00000643072.1:c.1145A>C	ENSP00000496691.1:p.His382Pro
ENST00000643362.1:c.911A>C	ENSP00000496398.1:p.His304Pro
ENST00000643583.1:c.1298A>C	ENSP00000494685.1:p.His433Pro
ENST00000643875.1:c.1298A>C	ENSP00000495158.1:p.His433Pro
ENST00000644097.1:c.1295A>C	ENSP00000494682.1:p.His432Pro
ENST00000644184.1:c.35A>C	ENSP00000495428.1:p.His12Pro
ENST00000644255.1:c.*1065A>C	ENSP00000493608.1:n.*1065A>C
ENST00000644319.1:n.1673A>C
ENST00000645901.1:n.2149A>C
ENST00000646391.1:c.*1068A>C	ENSP00000494104.1:n.*1068A>C
ENST00000646625.1:c.1298A>C	ENSP00000496263.1:p.His433Pro
ENST00000647279.1:c.*537A>C	ENSP00000494502.1:n.*537A>C
ENST00000647506.1:n.2174A>C
ENST00000647534.1:n.362A>C
ENST00000298552.7:c.1298A>C	ENSP00000298552.3:p.His433Pro
ENST00000440111.6:c.1298A>C	ENSP00000394524.2:p.His433Pro
ENST00000545250.5:c.1145A>C	ENSP00000444017.1:p.His382Pro
NM_000368.4:c.1298A>C , LRG_486t1:c.1298A>C	NP_000359.1:p.His433Pro
NM_001162426.1:c.1295A>C	NP_001155898.1:p.His432Pro
NM_001162427.1:c.1145A>C	NP_001155899.1:p.His382Pro
XM_005272211.1:c.1298A>C	XP_005272268.1:p.His433Pro
XM_006717271.1:c.1298A>C	XP_006717334.1:p.His433Pro
XM_006717272.2:c.1298A>C	XP_006717335.1:p.His433Pro
XM_011518979.1:c.1298A>C	XP_011517281.1:p.His433Pro
NM_001362177.1:c.935A>C	NP_001349106.1:p.His312Pro
XM_011518979.2:c.1298A>C	XP_011517281.1:p.His433Pro
XM_017015096.1:c.1298A>C	XP_016870585.1:p.His433Pro
XM_017015097.1:c.1298A>C	XP_016870586.1:p.His433Pro
XM_017015098.1:c.1295A>C	XP_016870587.1:p.His432Pro
XM_017015100.1:c.935A>C	XP_016870589.1:p.His312Pro
XM_017015101.1:c.932A>C	XP_016870590.1:p.His311Pro
NM_000368.5:c.1298A>C MANE Select	NP_000359.1:p.His433Pro
NM_001162426.2:c.1295A>C	NP_001155898.1:p.His432Pro
NM_001162427.2:c.1145A>C	NP_001155899.1:p.His382Pro
NM_001362177.2:c.935A>C	NP_001349106.1:p.His312Pro