Canonical Allele Identifier: CA2658520114
Gene: SPAST HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32064286_32064287insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG , CM000664.2:g.32064286_32064287insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG GRCh38
NC_000002.11:g.32289355_32289356insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG , CM000664.1:g.32289355_32289356insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG GRCh37
NC_000002.10:g.32142859_32142860insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG NCBI36
NG_008730.1:g.5676_5677insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG , LRG_714:g.5676_5677insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG ENSP00000515816.1:n.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGG...
ENST00000315285.9:c.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG MANE Select ENSP00000320885.3:n.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGG...
ENST00000621856.2:c.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG ENSP00000482496.2:n.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGG...
ENST00000642281.1:c.299+40_299+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG
ENST00000642455.1:c.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG ENSP00000493827.1:n.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGG...
ENST00000642751.1:c.285+40_285+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG
ENST00000642999.1:c.157+40_157+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG ENSP00000496589.1:n.157+40_157+41insAAGGGGGGGGGGGGGGGGGGGGGGG...
ENST00000644408.1:c.291+40_291+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG
ENST00000644954.1:c.157+40_157+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG ENSP00000494312.1:n.157+40_157+41insAAGGGGGGGGGGGGGGGGGGGGGGG...
ENST00000645400.1:c.256+40_256+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG ENSP00000496306.1:n.256+40_256+41insAAGGGGGGGGGGGGGGGGGGGGGGG...
ENST00000645671.1:c.36+40_36+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG
ENST00000646082.1:c.249+40_249+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG
ENST00000646571.1:c.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG ENSP00000495015.1:n.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGG...
ENST00000315285.7:c.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG ENSP00000320885.3:n.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGG...
ENST00000345662.5:c.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG ENSP00000340817.1:n.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGG...
ENST00000615843.4:c.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG ENSP00000480893.1:n.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGG...
ENST00000621856.1:c.157+40_157+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG ENSP00000482496.1:n.157+40_157+41insAAGGGGGGGGGGGGGGGGGGGGGGG...
NM_014946.3:c.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG , LRG_714t1:c.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG NP_055761.2:n.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGC...
NM_199436.1:c.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG NP_955468.1:n.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGC...
XM_005264516.3:c.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG XP_005264573.1:n.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGG...
XM_011533067.1:c.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG XP_011531369.1:n.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGG...
NM_001363823.1:c.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG NP_001350752.1:n.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGG...
NM_001363875.1:c.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG NP_001350804.1:n.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGG...
XM_005264516.5:c.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG XP_005264573.1:n.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGG...
XM_011533067.2:c.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG XP_011531369.1:n.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGG...
XM_017004778.2:c.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG XP_016860267.1:n.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGG...
NM_001363823.2:c.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG NP_001350752.1:n.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGG...
NM_001363875.2:c.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG NP_001350804.1:n.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGG...
NM_001377959.1:c.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG NP_001364888.1:n.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGG...
NM_014946.4:c.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG MANE Select NP_055761.2:n.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGC...
NM_199436.2:c.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGCGGG NP_955468.1:n.415+40_415+41insAAGGGGGGGGGGGGGGGGGGGGGGGGGGGGC...