Canonical Allele Identifier: CA531769490
Gene: SPAST HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32064274_32064275insGGGGGGGGGGCGG , CM000664.2:g.32064274_32064275insGGGGGGGGGGCGG GRCh38
NC_000002.11:g.32289343_32289344insGGGGGGGGGGCGG , CM000664.1:g.32289343_32289344insGGGGGGGGGGCGG GRCh37
NC_000002.10:g.32142847_32142848insGGGGGGGGGGCGG NCBI36
NG_008730.1:g.5664_5665insGGGGGGGGGGCGG , LRG_714:g.5664_5665insGGGGGGGGGGCGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.415+28_415+29insGGGGGGGGGGCGG ENSP00000515816.1:n.415+28_415+29insGGGGGGGGGGCGG
ENST00000315285.9:c.415+28_415+29insGGGGGGGGGGCGG MANE Select ENSP00000320885.3:n.415+28_415+29insGGGGGGGGGGCGG
ENST00000621856.2:c.415+28_415+29insGGGGGGGGGGCGG ENSP00000482496.2:n.415+28_415+29insGGGGGGGGGGCGG
ENST00000642281.1:c.299+28_299+29insGGGGGGGGGGCGG
ENST00000642455.1:c.415+28_415+29insGGGGGGGGGGCGG ENSP00000493827.1:n.415+28_415+29insGGGGGGGGGGCGG
ENST00000642751.1:c.285+28_285+29insGGGGGGGGGGCGG
ENST00000642999.1:c.157+28_157+29insGGGGGGGGGGCGG ENSP00000496589.1:n.157+28_157+29insGGGGGGGGGGCGG
ENST00000644408.1:c.291+28_291+29insGGGGGGGGGGCGG
ENST00000644954.1:c.157+28_157+29insGGGGGGGGGGCGG ENSP00000494312.1:n.157+28_157+29insGGGGGGGGGGCGG
ENST00000645400.1:c.256+28_256+29insGGGGGGGGGGCGG ENSP00000496306.1:n.256+28_256+29insGGGGGGGGGGCGG
ENST00000645671.1:c.36+28_36+29insGGGGGGGGGGCGG
ENST00000646082.1:c.249+28_249+29insGGGGGGGGGGCGG
ENST00000646571.1:c.415+28_415+29insGGGGGGGGGGCGG ENSP00000495015.1:n.415+28_415+29insGGGGGGGGGGCGG
ENST00000315285.7:c.415+28_415+29insGGGGGGGGGGCGG ENSP00000320885.3:n.415+28_415+29insGGGGGGGGGGCGG
ENST00000345662.5:c.415+28_415+29insGGGGGGGGGGCGG ENSP00000340817.1:n.415+28_415+29insGGGGGGGGGGCGG
ENST00000615843.4:c.415+28_415+29insGGGGGGGGGGCGG ENSP00000480893.1:n.415+28_415+29insGGGGGGGGGGCGG
ENST00000621856.1:c.157+28_157+29insGGGGGGGGGGCGG ENSP00000482496.1:n.157+28_157+29insGGGGGGGGGGCGG
NM_014946.3:c.415+28_415+29insGGGGGGGGGGCGG , LRG_714t1:c.415+28_415+29insGGGGGGGGGGCGG NP_055761.2:n.415+28_415+29insGGGGGGGGGGCGG
NM_199436.1:c.415+28_415+29insGGGGGGGGGGCGG NP_955468.1:n.415+28_415+29insGGGGGGGGGGCGG
XM_005264516.3:c.415+28_415+29insGGGGGGGGGGCGG XP_005264573.1:n.415+28_415+29insGGGGGGGGGGCGG
XM_011533067.1:c.415+28_415+29insGGGGGGGGGGCGG XP_011531369.1:n.415+28_415+29insGGGGGGGGGGCGG
NM_001363823.1:c.415+28_415+29insGGGGGGGGGGCGG NP_001350752.1:n.415+28_415+29insGGGGGGGGGGCGG
NM_001363875.1:c.415+28_415+29insGGGGGGGGGGCGG NP_001350804.1:n.415+28_415+29insGGGGGGGGGGCGG
XM_005264516.5:c.415+28_415+29insGGGGGGGGGGCGG XP_005264573.1:n.415+28_415+29insGGGGGGGGGGCGG
XM_011533067.2:c.415+28_415+29insGGGGGGGGGGCGG XP_011531369.1:n.415+28_415+29insGGGGGGGGGGCGG
XM_017004778.2:c.415+28_415+29insGGGGGGGGGGCGG XP_016860267.1:n.415+28_415+29insGGGGGGGGGGCGG
NM_001363823.2:c.415+28_415+29insGGGGGGGGGGCGG NP_001350752.1:n.415+28_415+29insGGGGGGGGGGCGG
NM_001363875.2:c.415+28_415+29insGGGGGGGGGGCGG NP_001350804.1:n.415+28_415+29insGGGGGGGGGGCGG
NM_001377959.1:c.415+28_415+29insGGGGGGGGGGCGG NP_001364888.1:n.415+28_415+29insGGGGGGGGGGCGG
NM_014946.4:c.415+28_415+29insGGGGGGGGGGCGG MANE Select NP_055761.2:n.415+28_415+29insGGGGGGGGGGCGG
NM_199436.2:c.415+28_415+29insGGGGGGGGGGCGG NP_955468.1:n.415+28_415+29insGGGGGGGGGGCGG