Canonical Allele Identifier: CA005869

Gene: TSC1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.132903805G>T , CM000671.2:g.132903805G>T	GRCh38
NC_000009.11:g.135779192G>T , CM000671.1:g.135779192G>T	GRCh37
NC_000009.10:g.134769013G>T	NCBI36
NG_012386.1:g.45829C>A , LRG_486:g.45829C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475903.7:c.2051C>A	ENSP00000496126.2:p.Ser684Ter
ENST00000490179.4:c.2054C>A	ENSP00000495533.2:p.Ser685Ter
ENST00000642261.2:c.2054C>A	ENSP00000494743.2:p.Ser685Ter
ENST00000643275.2:c.2010C>A	ENSP00000495598.2:p.Phe670Leu
ENST00000643362.2:c.1667C>A	ENSP00000496398.2:p.Ser556Ter
ENST00000643625.2:c.2041+606C>A	ENSP00000495546.2:n.2041+606C>A
ENST00000643691.2:c.1691C>A	ENSP00000494916.2:p.Ser564Ter
ENST00000644184.2:c.2054C>A	ENSP00000495428.2:p.Ser685Ter
ENST00000645129.2:c.1898C>A	ENSP00000493639.2:p.Ser633Ter
ENST00000646440.2:c.2054C>A	ENSP00000495830.2:p.Ser685Ter
ENST00000298552.9:c.2054C>A MANE Select	ENSP00000298552.3:p.Ser685Ter
ENST00000642261.1:c.118C>A
ENST00000642617.1:c.2051C>A	ENSP00000493773.1:p.Ser684Ter
ENST00000642627.1:c.2039-3C>A	ENSP00000496772.1:n.2039-3C>A
ENST00000642811.1:c.*1824C>A	ENSP00000495554.1:n.*1824C>A
ENST00000643072.1:c.1901C>A	ENSP00000496691.1:p.Ser634Ter
ENST00000643275.1:c.528C>A	ENSP00000495598.1:p.Phe176Leu
ENST00000643583.1:c.2042-3C>A	ENSP00000494685.1:n.2042-3C>A
ENST00000643625.1:c.85+606C>A	ENSP00000495546.1:n.85+606C>A
ENST00000643875.1:c.2054C>A	ENSP00000495158.1:p.Ser685Ter
ENST00000644097.1:c.2051C>A	ENSP00000494682.1:p.Ser684Ter
ENST00000644184.1:c.791C>A	ENSP00000495428.1:p.Ser264Ter
ENST00000644255.1:c.*1821C>A	ENSP00000493608.1:n.*1821C>A
ENST00000644319.1:n.2429C>A
ENST00000644882.1:n.1009C>A
ENST00000645901.1:n.2905C>A
ENST00000646391.1:c.*1824C>A	ENSP00000494104.1:n.*1824C>A
ENST00000646625.1:c.2054C>A	ENSP00000496263.1:p.Ser685Ter
ENST00000647262.1:n.1019C>A
ENST00000647279.1:c.*1293C>A	ENSP00000494502.1:n.*1293C>A
ENST00000647506.1:n.2930C>A
ENST00000647534.1:n.1118C>A
ENST00000298552.7:c.2054C>A	ENSP00000298552.3:p.Ser685Ter
ENST00000440111.6:c.2054C>A	ENSP00000394524.2:p.Ser685Ter
ENST00000545250.5:c.1901C>A	ENSP00000444017.1:p.Ser634Ter
NM_000368.4:c.2054C>A , LRG_486t1:c.2054C>A	NP_000359.1:p.Ser685Ter
NM_001162426.1:c.2051C>A	NP_001155898.1:p.Ser684Ter
NM_001162427.1:c.1901C>A	NP_001155899.1:p.Ser634Ter
XM_005272211.1:c.2054C>A	XP_005272268.1:p.Ser685Ter
XM_006717271.1:c.2054C>A	XP_006717334.1:p.Ser685Ter
XM_011518979.1:c.2054C>A	XP_011517281.1:p.Ser685Ter
NM_001362177.1:c.1691C>A	NP_001349106.1:p.Ser564Ter
XM_011518979.2:c.2054C>A	XP_011517281.1:p.Ser685Ter
XM_017015096.1:c.2054C>A	XP_016870585.1:p.Ser685Ter
XM_017015097.1:c.2054C>A	XP_016870586.1:p.Ser685Ter
XM_017015098.1:c.2051C>A	XP_016870587.1:p.Ser684Ter
XM_017015100.1:c.1691C>A	XP_016870589.1:p.Ser564Ter
XM_017015101.1:c.1688C>A	XP_016870590.1:p.Ser563Ter
NM_000368.5:c.2054C>A MANE Select	NP_000359.1:p.Ser685Ter
NM_001162426.2:c.2051C>A	NP_001155898.1:p.Ser684Ter
NM_001162427.2:c.1901C>A	NP_001155899.1:p.Ser634Ter
NM_001362177.2:c.1691C>A	NP_001349106.1:p.Ser564Ter