Canonical Allele Identifier: CA2658526616
Gene: SPAST HGNC NCBI

Linked Data

gnomAD v4: 2-32126928-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32126928C>T , CM000664.2:g.32126928C>T GRCh38
NC_000002.11:g.32351997C>T , CM000664.1:g.32351997C>T GRCh37
NC_000002.10:g.32205501C>T NCBI36
NG_008730.1:g.68318C>T , LRG_714:g.68318C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.*759-20C>T ENSP00000515816.1:n.*759-20C>T
ENST00000315285.9:c.1099-20C>T MANE Select ENSP00000320885.3:n.1099-20C>T
ENST00000621856.2:c.1096-20C>T ENSP00000482496.2:n.1096-20C>T
ENST00000642281.1:c.983-9635C>T
ENST00000642455.1:c.1000-20C>T ENSP00000493827.1:n.1000-20C>T
ENST00000642751.1:c.873-20C>T
ENST00000642999.1:c.841-20C>T ENSP00000496589.1:n.841-20C>T
ENST00000643327.1:c.258-20C>T
ENST00000643334.1:c.679-20C>T
ENST00000644408.1:c.975-20C>T
ENST00000644954.1:c.745-20C>T ENSP00000494312.1:n.745-20C>T
ENST00000645159.1:n.431C>T
ENST00000645550.1:n.292C>T
ENST00000645671.1:c.549-20C>T
ENST00000645730.1:c.446-20C>T
ENST00000646082.1:c.745-20C>T
ENST00000646571.1:c.1003-20C>T ENSP00000495015.1:n.1003-20C>T
ENST00000647007.1:n.791-20C>T
ENST00000647133.1:c.674-1480C>T
ENST00000315285.7:c.1099-20C>T ENSP00000320885.3:n.1099-20C>T
ENST00000345662.5:c.1003-20C>T ENSP00000340817.1:n.1003-20C>T
ENST00000615843.4:c.1099-20C>T ENSP00000480893.1:n.1099-20C>T
ENST00000621856.1:c.841-20C>T ENSP00000482496.1:n.841-20C>T
NM_014946.3:c.1099-20C>T , LRG_714t1:c.1099-20C>T NP_055761.2:n.1099-20C>T
NM_199436.1:c.1003-20C>T NP_955468.1:n.1003-20C>T
XM_005264516.3:c.1096-20C>T XP_005264573.1:n.1096-20C>T
XM_011533067.1:c.1099-20C>T XP_011531369.1:n.1099-20C>T
NM_001363823.1:c.1096-20C>T NP_001350752.1:n.1096-20C>T
NM_001363875.1:c.1000-20C>T NP_001350804.1:n.1000-20C>T
XM_005264516.5:c.1096-20C>T XP_005264573.1:n.1096-20C>T
XM_011533067.2:c.1099-20C>T XP_011531369.1:n.1099-20C>T
XM_017004778.2:c.1003-20C>T XP_016860267.1:n.1003-20C>T
NM_001363823.2:c.1096-20C>T NP_001350752.1:n.1096-20C>T
NM_001363875.2:c.1000-20C>T NP_001350804.1:n.1000-20C>T
NM_001377959.1:c.1003-20C>T NP_001364888.1:n.1003-20C>T
NM_014946.4:c.1099-20C>T MANE Select NP_055761.2:n.1099-20C>T
NM_199436.2:c.1003-20C>T NP_955468.1:n.1003-20C>T