Canonical Allele Identifier: CA1242506954
Gene: SPAST HGNC NCBI

Linked Data

dbSNP Id: rs1679914497

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32147187T>A , CM000664.2:g.32147187T>A GRCh38
NC_000002.11:g.32372256T>A , CM000664.1:g.32372256T>A GRCh37
NC_000002.10:g.32225760T>A NCBI36
NG_008730.1:g.88577T>A , LRG_714:g.88577T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.*1348-31T>A ENSP00000515816.1:n.*1348-31T>A
ENST00000315285.9:c.1688-31T>A MANE Select ENSP00000320885.3:n.1688-31T>A
ENST00000621856.2:c.1685-31T>A ENSP00000482496.2:n.1685-31T>A
ENST00000642281.1:c.1425-31T>A
ENST00000642455.1:c.1589-31T>A ENSP00000493827.1:n.1589-31T>A
ENST00000642751.1:c.1391-31T>A
ENST00000642999.1:c.1430-31T>A ENSP00000496589.1:n.1430-31T>A
ENST00000643334.1:c.1268-31T>A
ENST00000644408.1:c.1564-8T>A
ENST00000644954.1:c.1334-31T>A ENSP00000494312.1:n.1334-31T>A
ENST00000645159.1:n.2425-31T>A
ENST00000645671.1:c.1067-31T>A
ENST00000645730.1:c.867-31T>A
ENST00000646082.1:c.1334-31T>A
ENST00000646571.1:c.1592-31T>A ENSP00000495015.1:n.1592-31T>A
ENST00000647007.1:n.1380-31T>A
ENST00000647133.1:c.1188-31T>A
ENST00000315285.7:c.1688-31T>A ENSP00000320885.3:n.1688-31T>A
ENST00000345662.5:c.1592-31T>A ENSP00000340817.1:n.1592-31T>A
ENST00000615843.4:c.1688-31T>A ENSP00000480893.1:n.1688-31T>A
ENST00000621856.1:c.1430-31T>A ENSP00000482496.1:n.1430-31T>A
NM_014946.3:c.1688-31T>A , LRG_714t1:c.1688-31T>A NP_055761.2:n.1688-31T>A
NM_199436.1:c.1592-31T>A NP_955468.1:n.1592-31T>A
XM_005264516.3:c.1685-31T>A XP_005264573.1:n.1685-31T>A
XM_011533067.1:c.1617-31T>A XP_011531369.1:n.1617-31T>A
NM_001363823.1:c.1685-31T>A NP_001350752.1:n.1685-31T>A
NM_001363875.1:c.1589-31T>A NP_001350804.1:n.1589-31T>A
XM_005264516.5:c.1685-31T>A XP_005264573.1:n.1685-31T>A
XM_011533067.2:c.1617-31T>A XP_011531369.1:n.1617-31T>A
XM_017004778.2:c.1521-31T>A XP_016860267.1:n.1521-31T>A
NM_001363823.2:c.1685-31T>A NP_001350752.1:n.1685-31T>A
NM_001363875.2:c.1589-31T>A NP_001350804.1:n.1589-31T>A
NM_001377959.1:c.1521-31T>A NP_001364888.1:n.1521-31T>A
NM_014946.4:c.1688-31T>A MANE Select NP_055761.2:n.1688-31T>A
NM_199436.2:c.1592-31T>A NP_955468.1:n.1592-31T>A