Canonical Allele Identifier: CA027469

Gene: TSC1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132910579G>C , CM000671.2:g.132910579G>C	GRCh38
NC_000009.11:g.135785966G>C , CM000671.1:g.135785966G>C	GRCh37
NC_000009.10:g.134775787G>C	NCBI36
NG_012386.1:g.39055C>G , LRG_486:g.39055C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000368.5:c.1255C>G MANE Select	NP_000359.1:p.Pro419Ala
ENST00000298552.9:c.1255C>G MANE Select	ENSP00000298552.3:p.Pro419Ala
NM_000368.4:c.1255C>G , LRG_486t1:c.1255C>G	NP_000359.1:p.Pro419Ala
NM_001162426.1:c.1252C>G	NP_001155898.1:p.Pro418Ala
NM_001162426.2:c.1252C>G	NP_001155898.1:p.Pro418Ala
NM_001162427.1:c.1102C>G	NP_001155899.1:p.Pro368Ala
NM_001162427.2:c.1102C>G	NP_001155899.1:p.Pro368Ala
NM_001362177.1:c.892C>G	NP_001349106.1:p.Pro298Ala
NM_001362177.2:c.892C>G	NP_001349106.1:p.Pro298Ala
ENST00000298552.7:c.1255C>G	ENSP00000298552.3:p.Pro419Ala
ENST00000440111.6:c.1255C>G	ENSP00000394524.2:p.Pro419Ala
ENST00000475903.7:c.1252C>G	ENSP00000496126.2:p.Pro418Ala
ENST00000490179.4:c.1255C>G	ENSP00000495533.2:p.Pro419Ala
ENST00000493467.5:n.1451C>G
ENST00000493467.6:n.526C>G
ENST00000545250.5:c.1102C>G	ENSP00000444017.1:p.Pro368Ala
ENST00000642261.2:c.1255C>G	ENSP00000494743.2:p.Pro419Ala
ENST00000642344.1:c.*996C>G	ENSP00000494847.1:n.*996C>G
ENST00000642617.1:c.1252C>G	ENSP00000493773.1:p.Pro418Ala
ENST00000642627.1:c.1252C>G	ENSP00000496772.1:p.Pro418Ala
ENST00000642646.1:c.1255C>G	ENSP00000496292.1:p.Pro419Ala
ENST00000642745.1:c.1255C>G	ENSP00000493963.1:p.Pro419Ala
ENST00000642811.1:c.*1025C>G	ENSP00000495554.1:n.*1025C>G
ENST00000643072.1:c.1102C>G	ENSP00000496691.1:p.Pro368Ala
ENST00000643275.2:c.1255C>G	ENSP00000495598.2:p.Pro419Ala
ENST00000643362.1:c.876+874C>G	ENSP00000496398.1:n.876+874C>G
ENST00000643362.2:c.876+874C>G	ENSP00000496398.2:n.876+874C>G
ENST00000643583.1:c.1255C>G	ENSP00000494685.1:p.Pro419Ala
ENST00000643625.2:c.1255C>G	ENSP00000495546.2:p.Pro419Ala
ENST00000643691.2:c.892C>G	ENSP00000494916.2:p.Pro298Ala
ENST00000643875.1:c.1255C>G	ENSP00000495158.1:p.Pro419Ala
ENST00000644097.1:c.1252C>G	ENSP00000494682.1:p.Pro418Ala
ENST00000644184.2:c.1255C>G	ENSP00000495428.2:p.Pro419Ala
ENST00000644255.1:c.*1022C>G	ENSP00000493608.1:n.*1022C>G
ENST00000644319.1:n.1630C>G
ENST00000644997.1:c.*909C>G	ENSP00000495654.1:n.*909C>G
ENST00000645129.2:c.1099C>G	ENSP00000493639.2:p.Pro367Ala
ENST00000645150.1:c.1255C>G	ENSP00000494365.1:p.Pro419Ala
ENST00000645901.1:n.2106C>G
ENST00000646391.1:c.*1025C>G	ENSP00000494104.1:n.*1025C>G
ENST00000646440.2:c.1255C>G	ENSP00000495830.2:p.Pro419Ala
ENST00000646625.1:c.1255C>G	ENSP00000496263.1:p.Pro419Ala
ENST00000647078.1:c.*149C>G	ENSP00000496066.1:n.*149C>G
ENST00000647078.2:c.*149C>G	ENSP00000496066.1:n.*149C>G
ENST00000647279.1:c.*494C>G	ENSP00000494502.1:n.*494C>G
ENST00000647462.1:c.1252C>G	ENSP00000495821.1:p.Pro418Ala
ENST00000647506.1:n.2131C>G
ENST00000647534.1:n.319C>G
XM_005272211.1:c.1255C>G	XP_005272268.1:p.Pro419Ala
XM_006717271.1:c.1255C>G	XP_006717334.1:p.Pro419Ala
XM_006717272.2:c.1255C>G	XP_006717335.1:p.Pro419Ala
XM_011518979.1:c.1255C>G	XP_011517281.1:p.Pro419Ala
XM_011518979.2:c.1255C>G	XP_011517281.1:p.Pro419Ala
XM_017015096.1:c.1255C>G	XP_016870585.1:p.Pro419Ala
XM_017015097.1:c.1255C>G	XP_016870586.1:p.Pro419Ala
XM_017015098.1:c.1252C>G	XP_016870587.1:p.Pro418Ala
XM_017015100.1:c.892C>G	XP_016870589.1:p.Pro298Ala
XM_017015101.1:c.889C>G	XP_016870590.1:p.Pro297Ala