Canonical Allele Identifier: CA425446885
Gene: SPAST HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.32353491T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32128422T>A , CM000664.2:g.32128422T>A GRCh38
NC_000002.11:g.32353491T>A , CM000664.1:g.32353491T>A GRCh37
NC_000002.10:g.32206995T>A NCBI36
NG_008730.1:g.69812T>A , LRG_714:g.69812T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.*848T>A ENSP00000515816.1:n.*848T>A
ENST00000315285.9:c.1188T>A MANE Select ENSP00000320885.3:p.Ala396=
ENST00000621856.2:c.1185T>A ENSP00000482496.2:p.Ala395=
ENST00000642281.1:c.983-8141T>A
ENST00000642455.1:c.1089T>A ENSP00000493827.1:p.Ala363=
ENST00000642751.1:c.962T>A
ENST00000642999.1:c.930T>A ENSP00000496589.1:p.Ala310=
ENST00000643327.1:c.347T>A
ENST00000643334.1:c.768T>A
ENST00000644408.1:c.1064T>A
ENST00000644954.1:c.834T>A ENSP00000494312.1:p.Ala278=
ENST00000645159.1:n.1925T>A
ENST00000645550.1:n.401T>A
ENST00000645671.1:c.638T>A
ENST00000645730.1:c.535T>A
ENST00000646082.1:c.834T>A
ENST00000646571.1:c.1092T>A ENSP00000495015.1:p.Ala364=
ENST00000647007.1:n.880T>A
ENST00000647133.1:c.688T>A
ENST00000315285.7:c.1188T>A ENSP00000320885.3:p.Ala396=
ENST00000345662.5:c.1092T>A ENSP00000340817.1:p.Ala364=
ENST00000615843.4:c.1188T>A ENSP00000480893.1:p.Ala396=
ENST00000621856.1:c.930T>A ENSP00000482496.1:p.Ala310=
NM_014946.3:c.1188T>A , LRG_714t1:c.1188T>A NP_055761.2:p.Ala396=
NM_199436.1:c.1092T>A NP_955468.1:p.Ala364=
XM_005264516.3:c.1185T>A XP_005264573.1:p.Ala395=
XM_011533067.1:c.1188T>A XP_011531369.1:p.Ala396=
NM_001363823.1:c.1185T>A NP_001350752.1:p.Ala395=
NM_001363875.1:c.1089T>A NP_001350804.1:p.Ala363=
XM_005264516.5:c.1185T>A XP_005264573.1:p.Ala395=
XM_011533067.2:c.1188T>A XP_011531369.1:p.Ala396=
XM_017004778.2:c.1092T>A XP_016860267.1:p.Ala364=
NM_001363823.2:c.1185T>A NP_001350752.1:p.Ala395=
NM_001363875.2:c.1089T>A NP_001350804.1:p.Ala363=
NM_001377959.1:c.1092T>A NP_001364888.1:p.Ala364=
NM_014946.4:c.1188T>A MANE Select NP_055761.2:p.Ala396=
NM_199436.2:c.1092T>A NP_955468.1:p.Ala364=