Canonical Allele Identifier: CA2241762901
Gene: SPG7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89553823C= , CM000678.2:g.89553823C= GRCh38
NC_000016.9:g.89620231C= , CM000678.1:g.89620231C= GRCh37
NC_000016.8:g.88147732C= NCBI36
NG_008082.1:g.50427C=

Transcript Alleles

HGVS Amino-acid change
ENST00000268704.7:c.1945C= ENSP00000268704.3:p.Arg649=
ENST00000561702.6:n.2638C=
ENST00000566682.2:c.1007C= ENSP00000461979.2:p.Pro336=
ENST00000569720.2:n.649C=
ENST00000569820.6:c.2239C=
ENST00000642226.1:n.2029C=
ENST00000642334.1:c.3384C=
ENST00000642814.1:n.1381C=
ENST00000642984.1:n.1689C=
ENST00000643105.1:c.2672C=
ENST00000643350.1:n.1380C=
ENST00000643409.1:n.2391C=
ENST00000643496.1:n.1783C=
ENST00000643649.1:c.1855C= ENSP00000494806.1:p.Arg619=
ENST00000643668.1:c.*2260C= ENSP00000494903.1:n.*2260C=
ENST00000643724.1:c.*1014C= ENSP00000496335.1:n.*1014C=
ENST00000643954.1:c.2865C=
ENST00000644171.1:n.2726C=
ENST00000644210.1:c.*538C= ENSP00000495675.1:n.*538C=
ENST00000644225.1:n.1983C=
ENST00000644281.1:n.2650C=
ENST00000644464.1:n.619C=
ENST00000644498.1:c.*1785C= ENSP00000496244.1:n.*1785C=
ENST00000644671.1:c.1623C=
ENST00000644751.1:c.1154C=
ENST00000644781.1:c.1921C= ENSP00000495473.1:p.Arg641=
ENST00000644901.1:c.*2360C= ENSP00000493797.1:n.*2360C=
ENST00000645042.1:c.*740C= ENSP00000493908.1:n.*740C=
ENST00000645063.1:c.1966C= ENSP00000493590.1:p.Arg656=
ENST00000645354.1:c.2726C=
ENST00000645392.1:n.2307C=
ENST00000645742.1:n.600C=
ENST00000645818.2:c.1966C= MANE Select ENSP00000495795.2:p.Arg656=
ENST00000645842.1:n.1811C=
ENST00000645886.1:c.1471C=
ENST00000645897.1:c.1504C= ENSP00000495293.1:p.Arg502=
ENST00000645952.1:n.1831C=
ENST00000645977.1:n.3084C=
ENST00000646005.1:n.1724C=
ENST00000646263.1:c.*839C= ENSP00000494119.1:n.*839C=
ENST00000646303.1:c.1834C= ENSP00000494160.1:p.Arg612=
ENST00000646399.1:c.2860C=
ENST00000646445.1:c.824C=
ENST00000646531.1:c.*589C= ENSP00000495185.1:n.*589C=
ENST00000646589.1:c.*1094C= ENSP00000494739.1:n.*1094C=
ENST00000646716.1:c.1018C= ENSP00000495593.1:p.Arg340=
ENST00000646826.1:c.*639C= ENSP00000495123.1:n.*639C=
ENST00000646930.1:c.*1895C= ENSP00000495219.1:n.*1895C=
ENST00000647032.1:c.1581C=
ENST00000647079.1:c.1558C= ENSP00000495967.1:p.Arg520=
ENST00000647123.1:n.1923C=
ENST00000647227.1:c.1604C=
ENST00000647302.1:n.2616C=
ENST00000647476.1:n.853C=
ENST00000647491.1:n.1710C=
ENST00000268704.6:c.1966C= ENSP00000268704.2:p.Arg656=
ENST00000561702.5:n.951C=
ENST00000561911.5:c.566C= ENSP00000457387.1:p.Pro189=
ENST00000566682.1:c.102C=
ENST00000569720.1:n.157C=
ENST00000569820.5:c.1208C=
ENST00000620811.4:c.*12C= ENSP00000478030.1:n.*12C=
NM_003119.3:c.1966C= NP_003110.1:p.Arg656=
XM_006721264.2:c.1966C= XP_006721327.1:p.Arg656=
NM_001363850.1:c.1966C= NP_001350779.1:p.Arg656=
XM_006721264.4:c.1966C= XP_006721327.1:p.Arg656=
XR_001751971.2:n.2315C=
XR_001751972.2:n.3602C=
NM_003119.4:c.1966C= MANE Select NP_003110.1:p.Arg656=