Canonical Allele Identifier: CA1242498143
Gene: SPAST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32128459G= , CM000664.2:g.32128459G= GRCh38
NC_000002.11:g.32353528G= , CM000664.1:g.32353528G= GRCh37
NC_000002.10:g.32207032G= NCBI36
NG_008730.1:g.69849G= , LRG_714:g.69849G=

Transcript Alleles

HGVS Amino-acid Change
NM_014946.4:c.1225G= MANE Select NP_055761.2:p.Ala409=
ENST00000315285.9:c.1225G= MANE Select ENSP00000320885.3:p.Ala409=
NM_001363823.1:c.1222G= NP_001350752.1:p.Ala408=
NM_001363823.2:c.1222G= NP_001350752.1:p.Ala408=
NM_001363875.1:c.1126G= NP_001350804.1:p.Ala376=
NM_001363875.2:c.1126G= NP_001350804.1:p.Ala376=
NM_001377959.1:c.1129G= NP_001364888.1:p.Ala377=
NM_014946.3:c.1225G= , LRG_714t1:c.1225G= NP_055761.2:p.Ala409=
NM_199436.1:c.1129G= NP_955468.1:p.Ala377=
NM_199436.2:c.1129G= NP_955468.1:p.Ala377=
ENST00000315285.7:c.1225G= ENSP00000320885.3:p.Ala409=
ENST00000345662.5:c.1129G= ENSP00000340817.1:p.Ala377=
ENST00000615843.4:c.1225G= ENSP00000480893.1:p.Ala409=
ENST00000621856.1:c.967G= ENSP00000482496.1:p.Ala323=
ENST00000621856.2:c.1222G= ENSP00000482496.2:p.Ala408=
ENST00000642281.1:c.983-8104G=
ENST00000642455.1:c.1126G= ENSP00000493827.1:p.Ala376=
ENST00000642751.1:c.999G=
ENST00000642999.1:c.967G= ENSP00000496589.1:p.Ala323=
ENST00000643327.1:c.384G=
ENST00000643334.1:c.805G=
ENST00000644408.1:c.1101G=
ENST00000644954.1:c.871G= ENSP00000494312.1:p.Ala291=
ENST00000645159.1:n.1962G=
ENST00000645550.1:n.438G=
ENST00000645671.1:c.675G=
ENST00000645730.1:c.572G=
ENST00000646082.1:c.871G=
ENST00000646571.1:c.1129G= ENSP00000495015.1:p.Ala377=
ENST00000647007.1:n.917G=
ENST00000647133.1:c.725G=
ENST00000704289.1:c.*885G= ENSP00000515816.1:n.*885G=
XM_005264516.3:c.1222G= XP_005264573.1:p.Ala408=
XM_005264516.5:c.1222G= XP_005264573.1:p.Ala408=
XM_011533067.1:c.1225G= XP_011531369.1:p.Ala409=
XM_011533067.2:c.1225G= XP_011531369.1:p.Ala409=
XM_017004778.2:c.1129G= XP_016860267.1:p.Ala377=