Canonical Allele Identifier: CA346501872
Gene: SPAST HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32136578A>C , CM000664.2:g.32136578A>C GRCh38
NC_000002.11:g.32361647A>C , CM000664.1:g.32361647A>C GRCh37
NC_000002.10:g.32215151A>C NCBI36
NG_008730.1:g.77968A>C , LRG_714:g.77968A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.*921A>C ENSP00000515816.1:n.*921A>C
ENST00000315285.9:c.1261A>C MANE Select ENSP00000320885.3:p.Lys421Gln
ENST00000621856.2:c.1258A>C ENSP00000482496.2:p.Lys420Gln
ENST00000642281.1:c.998A>C
ENST00000642455.1:c.1162A>C ENSP00000493827.1:p.Lys388Gln
ENST00000642751.1:c.1035A>C
ENST00000642999.1:c.1003A>C ENSP00000496589.1:p.Lys335Gln
ENST00000643327.1:c.420A>C
ENST00000643334.1:c.841A>C
ENST00000644408.1:c.1137A>C
ENST00000644954.1:c.907A>C ENSP00000494312.1:p.Lys303Gln
ENST00000645159.1:n.1998A>C
ENST00000645671.1:c.711A>C
ENST00000645730.1:c.593-531A>C
ENST00000646082.1:c.907A>C
ENST00000646571.1:c.1165A>C ENSP00000495015.1:p.Lys389Gln
ENST00000647007.1:n.953A>C
ENST00000647133.1:c.761A>C
ENST00000315285.7:c.1261A>C ENSP00000320885.3:p.Lys421Gln
ENST00000345662.5:c.1165A>C ENSP00000340817.1:p.Lys389Gln
ENST00000615843.4:c.1261A>C ENSP00000480893.1:p.Lys421Gln
ENST00000621856.1:c.1003A>C ENSP00000482496.1:p.Lys335Gln
NM_014946.3:c.1261A>C , LRG_714t1:c.1261A>C NP_055761.2:p.Lys421Gln
NM_199436.1:c.1165A>C NP_955468.1:p.Lys389Gln
XM_005264516.3:c.1258A>C XP_005264573.1:p.Lys420Gln
XM_011533067.1:c.1261A>C XP_011531369.1:p.Lys421Gln
NM_001363823.1:c.1258A>C NP_001350752.1:p.Lys420Gln
NM_001363875.1:c.1162A>C NP_001350804.1:p.Lys388Gln
XM_005264516.5:c.1258A>C XP_005264573.1:p.Lys420Gln
XM_011533067.2:c.1261A>C XP_011531369.1:p.Lys421Gln
XM_017004778.2:c.1165A>C XP_016860267.1:p.Lys389Gln
NM_001363823.2:c.1258A>C NP_001350752.1:p.Lys420Gln
NM_001363875.2:c.1162A>C NP_001350804.1:p.Lys388Gln
NM_001377959.1:c.1165A>C NP_001364888.1:p.Lys389Gln
NM_014946.4:c.1261A>C MANE Select NP_055761.2:p.Lys421Gln
NM_199436.2:c.1165A>C NP_955468.1:p.Lys389Gln