Canonical Allele Identifier: CA346502017
Gene: SPAST HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32136579A>G , CM000664.2:g.32136579A>G GRCh38
NC_000002.11:g.32361648A>G , CM000664.1:g.32361648A>G GRCh37
NC_000002.10:g.32215152A>G NCBI36
NG_008730.1:g.77969A>G , LRG_714:g.77969A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.*922A>G ENSP00000515816.1:n.*922A>G
ENST00000315285.9:c.1262A>G MANE Select ENSP00000320885.3:p.Lys421Arg
ENST00000621856.2:c.1259A>G ENSP00000482496.2:p.Lys420Arg
ENST00000642281.1:c.999A>G
ENST00000642455.1:c.1163A>G ENSP00000493827.1:p.Lys388Arg
ENST00000642751.1:c.1036A>G
ENST00000642999.1:c.1004A>G ENSP00000496589.1:p.Lys335Arg
ENST00000643327.1:c.421A>G
ENST00000643334.1:c.842A>G
ENST00000644408.1:c.1138A>G
ENST00000644954.1:c.908A>G ENSP00000494312.1:p.Lys303Arg
ENST00000645159.1:n.1999A>G
ENST00000645671.1:c.712A>G
ENST00000645730.1:c.593-530A>G
ENST00000646082.1:c.908A>G
ENST00000646571.1:c.1166A>G ENSP00000495015.1:p.Lys389Arg
ENST00000647007.1:n.954A>G
ENST00000647133.1:c.762A>G
ENST00000315285.7:c.1262A>G ENSP00000320885.3:p.Lys421Arg
ENST00000345662.5:c.1166A>G ENSP00000340817.1:p.Lys389Arg
ENST00000615843.4:c.1262A>G ENSP00000480893.1:p.Lys421Arg
ENST00000621856.1:c.1004A>G ENSP00000482496.1:p.Lys335Arg
NM_014946.3:c.1262A>G , LRG_714t1:c.1262A>G NP_055761.2:p.Lys421Arg
NM_199436.1:c.1166A>G NP_955468.1:p.Lys389Arg
XM_005264516.3:c.1259A>G XP_005264573.1:p.Lys420Arg
XM_011533067.1:c.1262A>G XP_011531369.1:p.Lys421Arg
NM_001363823.1:c.1259A>G NP_001350752.1:p.Lys420Arg
NM_001363875.1:c.1163A>G NP_001350804.1:p.Lys388Arg
XM_005264516.5:c.1259A>G XP_005264573.1:p.Lys420Arg
XM_011533067.2:c.1262A>G XP_011531369.1:p.Lys421Arg
XM_017004778.2:c.1166A>G XP_016860267.1:p.Lys389Arg
NM_001363823.2:c.1259A>G NP_001350752.1:p.Lys420Arg
NM_001363875.2:c.1163A>G NP_001350804.1:p.Lys388Arg
NM_001377959.1:c.1166A>G NP_001364888.1:p.Lys389Arg
NM_014946.4:c.1262A>G MANE Select NP_055761.2:p.Lys421Arg
NM_199436.2:c.1166A>G NP_955468.1:p.Lys389Arg