Canonical Allele Identifier: CA2658529118
Gene: SPAST HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32136465del , CM000664.2:g.32136465del GRCh38
NC_000002.11:g.32361534del , CM000664.1:g.32361534del GRCh37
NC_000002.10:g.32215038del NCBI36
NG_008730.1:g.77855del , LRG_714:g.77855del

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.*906-98del ENSP00000515816.1:n.*906-98del
ENST00000315285.9:c.1246-98del MANE Select ENSP00000320885.3:n.1246-98del
ENST00000621856.2:c.1243-98del ENSP00000482496.2:n.1243-98del
ENST00000642281.1:c.983-98del
ENST00000642455.1:c.1147-98del ENSP00000493827.1:n.1147-98del
ENST00000642751.1:c.1020-98del
ENST00000642999.1:c.988-98del ENSP00000496589.1:n.988-98del
ENST00000643327.1:c.405-98del
ENST00000643334.1:c.826-98del
ENST00000644408.1:c.1122-98del
ENST00000644954.1:c.892-98del ENSP00000494312.1:n.892-98del
ENST00000645159.1:n.1983-98del
ENST00000645671.1:c.696-98del
ENST00000645730.1:c.593-644del
ENST00000646082.1:c.892-98del
ENST00000646571.1:c.1150-98del ENSP00000495015.1:n.1150-98del
ENST00000647007.1:n.938-98del
ENST00000647133.1:c.746-98del
ENST00000315285.7:c.1246-98del ENSP00000320885.3:n.1246-98del
ENST00000345662.5:c.1150-98del ENSP00000340817.1:n.1150-98del
ENST00000615843.4:c.1246-98del ENSP00000480893.1:n.1246-98del
ENST00000621856.1:c.988-98del ENSP00000482496.1:n.988-98del
NM_014946.3:c.1246-98del , LRG_714t1:c.1246-98del NP_055761.2:n.1246-98del
NM_199436.1:c.1150-98del NP_955468.1:n.1150-98del
XM_005264516.3:c.1243-98del XP_005264573.1:n.1243-98del
XM_011533067.1:c.1246-98del XP_011531369.1:n.1246-98del
NM_001363823.1:c.1243-98del NP_001350752.1:n.1243-98del
NM_001363875.1:c.1147-98del NP_001350804.1:n.1147-98del
XM_005264516.5:c.1243-98del XP_005264573.1:n.1243-98del
XM_011533067.2:c.1246-98del XP_011531369.1:n.1246-98del
XM_017004778.2:c.1150-98del XP_016860267.1:n.1150-98del
NM_001363823.2:c.1243-98del NP_001350752.1:n.1243-98del
NM_001363875.2:c.1147-98del NP_001350804.1:n.1147-98del
NM_001377959.1:c.1150-98del NP_001364888.1:n.1150-98del
NM_014946.4:c.1246-98del MANE Select NP_055761.2:n.1246-98del
NM_199436.2:c.1150-98del NP_955468.1:n.1150-98del