Canonical Allele Identifier: CA2580066403
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1703284
ClinVar RCV Id: RCV002280406

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32128446_32128449delinsAAAA , CM000664.2:g.32128446_32128449delinsAAAA GRCh38
NC_000002.11:g.32353515_32353518delinsAAAA , CM000664.1:g.32353515_32353518delinsAAAA GRCh37
NC_000002.10:g.32207019_32207022delinsAAAA NCBI36
NG_008730.1:g.69836_69839delinsAAAA , LRG_714:g.69836_69839delinsAAAA

Transcript Alleles

HGVS Amino-acid change
ENST00000704289.1:c.*872_*875delinsAAAA ENSP00000515816.1:n.*872_*875delinsAAAA
ENST00000315285.9:c.1212_1215delinsAAAA MANE Select ENSP00000320885.3:p.Phe404_Asn405delinsLe...
ENST00000621856.2:c.1209_1212delinsAAAA ENSP00000482496.2:p.Phe403_Asn404delinsLe...
ENST00000642281.1:c.983-8117_983-8114delinsAAAA
ENST00000642455.1:c.1113_1116delinsAAAA ENSP00000493827.1:p.Phe371_Asn372delinsLe...
ENST00000642751.1:c.986_989delinsAAAA
ENST00000642999.1:c.954_957delinsAAAA ENSP00000496589.1:p.Phe318_Asn319delinsLe...
ENST00000643327.1:c.371_374delinsAAAA
ENST00000643334.1:c.792_795delinsAAAA
ENST00000644408.1:c.1088_1091delinsAAAA
ENST00000644954.1:c.858_861delinsAAAA ENSP00000494312.1:p.Phe286_Asn287delinsLe...
ENST00000645159.1:n.1949_1952delinsAAAA
ENST00000645550.1:n.425_428delinsAAAA
ENST00000645671.1:c.662_665delinsAAAA
ENST00000645730.1:c.559_562delinsAAAA
ENST00000646082.1:c.858_861delinsAAAA
ENST00000646571.1:c.1116_1119delinsAAAA ENSP00000495015.1:p.Phe372_Asn373delinsLe...
ENST00000647007.1:n.904_907delinsAAAA
ENST00000647133.1:c.712_715delinsAAAA
ENST00000315285.7:c.1212_1215delinsAAAA ENSP00000320885.3:p.Phe404_Asn405delinsLe...
ENST00000345662.5:c.1116_1119delinsAAAA ENSP00000340817.1:p.Phe372_Asn373delinsLe...
ENST00000615843.4:c.1212_1215delinsAAAA ENSP00000480893.1:p.Phe404_Asn405delinsLe...
ENST00000621856.1:c.954_957delinsAAAA ENSP00000482496.1:p.Phe318_Asn319delinsLe...
NM_014946.3:c.1212_1215delinsAAAA , LRG_714t1:c.1212_1215delinsAAAA NP_055761.2:p.Phe404_Asn405delinsLeuLys
NM_199436.1:c.1116_1119delinsAAAA NP_955468.1:p.Phe372_Asn373delinsLeuLys
XM_005264516.3:c.1209_1212delinsAAAA XP_005264573.1:p.Phe403_Asn404delinsLeuLy...
XM_011533067.1:c.1212_1215delinsAAAA XP_011531369.1:p.Phe404_Asn405delinsLeuLy...
NM_001363823.1:c.1209_1212delinsAAAA NP_001350752.1:p.Phe403_Asn404delinsLeuLy...
NM_001363875.1:c.1113_1116delinsAAAA NP_001350804.1:p.Phe371_Asn372delinsLeuLy...
XM_005264516.5:c.1209_1212delinsAAAA XP_005264573.1:p.Phe403_Asn404delinsLeuLy...
XM_011533067.2:c.1212_1215delinsAAAA XP_011531369.1:p.Phe404_Asn405delinsLeuLy...
XM_017004778.2:c.1116_1119delinsAAAA XP_016860267.1:p.Phe372_Asn373delinsLeuLy...
NM_001363823.2:c.1209_1212delinsAAAA NP_001350752.1:p.Phe403_Asn404delinsLeuLy...
NM_001363875.2:c.1113_1116delinsAAAA NP_001350804.1:p.Phe371_Asn372delinsLeuLy...
NM_001377959.1:c.1116_1119delinsAAAA NP_001364888.1:p.Phe372_Asn373delinsLeuLy...
NM_014946.4:c.1212_1215delinsAAAA MANE Select NP_055761.2:p.Phe404_Asn405delinsLeuLys
NM_199436.2:c.1116_1119delinsAAAA NP_955468.1:p.Phe372_Asn373delinsLeuLys