Canonical Allele Identifier: CA346602463
Gene: SPAST HGNC NCBI

Linked Data

dbSNP Id: rs1676415779
gnomAD v3: 2-32064220-C-T
gnomAD v4: 2-32064220-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32064220C>T , CM000664.2:g.32064220C>T GRCh38
NC_000002.11:g.32289289C>T , CM000664.1:g.32289289C>T GRCh37
NC_000002.10:g.32142793C>T NCBI36
NG_008730.1:g.5610C>T , LRG_714:g.5610C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.389C>T ENSP00000515816.1:p.Ala130Val
ENST00000315285.9:c.389C>T MANE Select ENSP00000320885.3:p.Ala130Val
ENST00000621856.2:c.389C>T ENSP00000482496.2:p.Ala130Val
ENST00000642281.1:c.273C>T
ENST00000642455.1:c.389C>T ENSP00000493827.1:p.Ala130Val
ENST00000642751.1:c.259C>T
ENST00000642999.1:c.131C>T ENSP00000496589.1:p.Ala44Val
ENST00000644408.1:c.265C>T
ENST00000644954.1:c.131C>T ENSP00000494312.1:p.Ala44Val
ENST00000645400.1:c.230C>T ENSP00000496306.1:p.Ala77Val
ENST00000645671.1:c.10C>T
ENST00000646082.1:c.223C>T
ENST00000646571.1:c.389C>T ENSP00000495015.1:p.Ala130Val
ENST00000315285.7:c.389C>T ENSP00000320885.3:p.Ala130Val
ENST00000345662.5:c.389C>T ENSP00000340817.1:p.Ala130Val
ENST00000615843.4:c.389C>T ENSP00000480893.1:p.Ala130Val
ENST00000621856.1:c.131C>T ENSP00000482496.1:p.Ala44Val
NM_014946.3:c.389C>T , LRG_714t1:c.389C>T NP_055761.2:p.Ala130Val
NM_199436.1:c.389C>T NP_955468.1:p.Ala130Val
XM_005264516.3:c.389C>T XP_005264573.1:p.Ala130Val
XM_011533067.1:c.389C>T XP_011531369.1:p.Ala130Val
NM_001363823.1:c.389C>T NP_001350752.1:p.Ala130Val
NM_001363875.1:c.389C>T NP_001350804.1:p.Ala130Val
XM_005264516.5:c.389C>T XP_005264573.1:p.Ala130Val
XM_011533067.2:c.389C>T XP_011531369.1:p.Ala130Val
XM_017004778.2:c.389C>T XP_016860267.1:p.Ala130Val
NM_001363823.2:c.389C>T NP_001350752.1:p.Ala130Val
NM_001363875.2:c.389C>T NP_001350804.1:p.Ala130Val
NM_001377959.1:c.389C>T NP_001364888.1:p.Ala130Val
NM_014946.4:c.389C>T MANE Select NP_055761.2:p.Ala130Val
NM_199436.2:c.389C>T NP_955468.1:p.Ala130Val