Canonical Allele Identifier: CA1242497322
Gene: SPAST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32126786G= , CM000664.2:g.32126786G= GRCh38
NC_000002.11:g.32351855G= , CM000664.1:g.32351855G= GRCh37
NC_000002.10:g.32205359G= NCBI36
NG_008730.1:g.68176G= , LRG_714:g.68176G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.*759-162G= ENSP00000515816.1:n.*759-162G=
ENST00000315285.9:c.1099-162G= MANE Select ENSP00000320885.3:n.1099-162G=
ENST00000621856.2:c.1096-162G= ENSP00000482496.2:n.1096-162G=
ENST00000642281.1:c.983-9777G=
ENST00000642455.1:c.1000-162G= ENSP00000493827.1:n.1000-162G=
ENST00000642751.1:c.873-162G=
ENST00000642999.1:c.841-162G= ENSP00000496589.1:n.841-162G=
ENST00000643327.1:c.258-162G=
ENST00000643334.1:c.679-162G=
ENST00000644408.1:c.975-162G=
ENST00000644954.1:c.745-162G= ENSP00000494312.1:n.745-162G=
ENST00000645159.1:n.289G=
ENST00000645550.1:n.150G=
ENST00000645671.1:c.549-162G=
ENST00000645730.1:c.446-162G=
ENST00000646082.1:c.745-162G=
ENST00000646571.1:c.1003-162G= ENSP00000495015.1:n.1003-162G=
ENST00000647007.1:n.791-162G=
ENST00000647133.1:c.674-1622G=
ENST00000315285.7:c.1099-162G= ENSP00000320885.3:n.1099-162G=
ENST00000345662.5:c.1003-162G= ENSP00000340817.1:n.1003-162G=
ENST00000615843.4:c.1099-162G= ENSP00000480893.1:n.1099-162G=
ENST00000621856.1:c.841-162G= ENSP00000482496.1:n.841-162G=
NM_014946.3:c.1099-162G= , LRG_714t1:c.1099-162G= NP_055761.2:n.1099-162G=
NM_199436.1:c.1003-162G= NP_955468.1:n.1003-162G=
XM_005264516.3:c.1096-162G= XP_005264573.1:n.1096-162G=
XM_011533067.1:c.1099-162G= XP_011531369.1:n.1099-162G=
NM_001363823.1:c.1096-162G= NP_001350752.1:n.1096-162G=
NM_001363875.1:c.1000-162G= NP_001350804.1:n.1000-162G=
XM_005264516.5:c.1096-162G= XP_005264573.1:n.1096-162G=
XM_011533067.2:c.1099-162G= XP_011531369.1:n.1099-162G=
XM_017004778.2:c.1003-162G= XP_016860267.1:n.1003-162G=
NM_001363823.2:c.1096-162G= NP_001350752.1:n.1096-162G=
NM_001363875.2:c.1000-162G= NP_001350804.1:n.1000-162G=
NM_001377959.1:c.1003-162G= NP_001364888.1:n.1003-162G=
NM_014946.4:c.1099-162G= MANE Select NP_055761.2:n.1099-162G=
NM_199436.2:c.1003-162G= NP_955468.1:n.1003-162G=