Canonical Allele Identifier: CA425446898
Gene: SPAST HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.32353506A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32128437A>T , CM000664.2:g.32128437A>T GRCh38
NC_000002.11:g.32353506A>T , CM000664.1:g.32353506A>T GRCh37
NC_000002.10:g.32207010A>T NCBI36
NG_008730.1:g.69827A>T , LRG_714:g.69827A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.*863A>T ENSP00000515816.1:n.*863A>T
ENST00000315285.9:c.1203A>T MANE Select ENSP00000320885.3:p.Ala401=
ENST00000621856.2:c.1200A>T ENSP00000482496.2:p.Ala400=
ENST00000642281.1:c.983-8126A>T
ENST00000642455.1:c.1104A>T ENSP00000493827.1:p.Ala368=
ENST00000642751.1:c.977A>T
ENST00000642999.1:c.945A>T ENSP00000496589.1:p.Ala315=
ENST00000643327.1:c.362A>T
ENST00000643334.1:c.783A>T
ENST00000644408.1:c.1079A>T
ENST00000644954.1:c.849A>T ENSP00000494312.1:p.Ala283=
ENST00000645159.1:n.1940A>T
ENST00000645550.1:n.416A>T
ENST00000645671.1:c.653A>T
ENST00000645730.1:c.550A>T
ENST00000646082.1:c.849A>T
ENST00000646571.1:c.1107A>T ENSP00000495015.1:p.Ala369=
ENST00000647007.1:n.895A>T
ENST00000647133.1:c.703A>T
ENST00000315285.7:c.1203A>T ENSP00000320885.3:p.Ala401=
ENST00000345662.5:c.1107A>T ENSP00000340817.1:p.Ala369=
ENST00000615843.4:c.1203A>T ENSP00000480893.1:p.Ala401=
ENST00000621856.1:c.945A>T ENSP00000482496.1:p.Ala315=
NM_014946.3:c.1203A>T , LRG_714t1:c.1203A>T NP_055761.2:p.Ala401=
NM_199436.1:c.1107A>T NP_955468.1:p.Ala369=
XM_005264516.3:c.1200A>T XP_005264573.1:p.Ala400=
XM_011533067.1:c.1203A>T XP_011531369.1:p.Ala401=
NM_001363823.1:c.1200A>T NP_001350752.1:p.Ala400=
NM_001363875.1:c.1104A>T NP_001350804.1:p.Ala368=
XM_005264516.5:c.1200A>T XP_005264573.1:p.Ala400=
XM_011533067.2:c.1203A>T XP_011531369.1:p.Ala401=
XM_017004778.2:c.1107A>T XP_016860267.1:p.Ala369=
NM_001363823.2:c.1200A>T NP_001350752.1:p.Ala400=
NM_001363875.2:c.1104A>T NP_001350804.1:p.Ala368=
NM_001377959.1:c.1107A>T NP_001364888.1:p.Ala369=
NM_014946.4:c.1203A>T MANE Select NP_055761.2:p.Ala401=
NM_199436.2:c.1107A>T NP_955468.1:p.Ala369=