Canonical Allele Identifier: CA1242498107
Gene: SPAST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32128393T= , CM000664.2:g.32128393T= GRCh38
NC_000002.11:g.32353462T= , CM000664.1:g.32353462T= GRCh37
NC_000002.10:g.32206966T= NCBI36
NG_008730.1:g.69783T= , LRG_714:g.69783T=

Transcript Alleles

HGVS Amino-acid change
ENST00000704289.1:c.*834-15T= ENSP00000515816.1:n.*834-15T=
ENST00000315285.9:c.1174-15T= MANE Select ENSP00000320885.3:n.1174-15T=
ENST00000621856.2:c.1171-15T= ENSP00000482496.2:n.1171-15T=
ENST00000642281.1:c.983-8170T=
ENST00000642455.1:c.1075-15T= ENSP00000493827.1:n.1075-15T=
ENST00000642751.1:c.948-15T=
ENST00000642999.1:c.916-15T= ENSP00000496589.1:n.916-15T=
ENST00000643327.1:c.333-15T=
ENST00000643334.1:c.754-15T=
ENST00000644408.1:c.1050-15T=
ENST00000644954.1:c.820-15T= ENSP00000494312.1:n.820-15T=
ENST00000645159.1:n.1896T=
ENST00000645550.1:n.387-15T=
ENST00000645671.1:c.624-15T=
ENST00000645730.1:c.521-15T=
ENST00000646082.1:c.820-15T=
ENST00000646571.1:c.1078-15T= ENSP00000495015.1:n.1078-15T=
ENST00000647007.1:n.866-15T=
ENST00000647133.1:c.674-15T=
ENST00000315285.7:c.1174-15T= ENSP00000320885.3:n.1174-15T=
ENST00000345662.5:c.1078-15T= ENSP00000340817.1:n.1078-15T=
ENST00000615843.4:c.1174-15T= ENSP00000480893.1:n.1174-15T=
ENST00000621856.1:c.916-15T= ENSP00000482496.1:n.916-15T=
NM_014946.3:c.1174-15T= , LRG_714t1:c.1174-15T= NP_055761.2:n.1174-15T=
NM_199436.1:c.1078-15T= NP_955468.1:n.1078-15T=
XM_005264516.3:c.1171-15T= XP_005264573.1:n.1171-15T=
XM_011533067.1:c.1174-15T= XP_011531369.1:n.1174-15T=
NM_001363823.1:c.1171-15T= NP_001350752.1:n.1171-15T=
NM_001363875.1:c.1075-15T= NP_001350804.1:n.1075-15T=
XM_005264516.5:c.1171-15T= XP_005264573.1:n.1171-15T=
XM_011533067.2:c.1174-15T= XP_011531369.1:n.1174-15T=
XM_017004778.2:c.1078-15T= XP_016860267.1:n.1078-15T=
NM_001363823.2:c.1171-15T= NP_001350752.1:n.1171-15T=
NM_001363875.2:c.1075-15T= NP_001350804.1:n.1075-15T=
NM_001377959.1:c.1078-15T= NP_001364888.1:n.1078-15T=
NM_014946.4:c.1174-15T= MANE Select NP_055761.2:n.1174-15T=
NM_199436.2:c.1078-15T= NP_955468.1:n.1078-15T=