Canonical Allele Identifier: CA346603580
Gene: SPAST HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32089591G>C , CM000664.2:g.32089591G>C GRCh38
NC_000002.11:g.32314660G>C , CM000664.1:g.32314660G>C GRCh37
NC_000002.10:g.32168164G>C NCBI36
NG_008730.1:g.30981G>C , LRG_714:g.30981G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000704289.1:c.*232G>C ENSP00000515816.1:n.*232G>C
ENST00000315285.9:c.572G>C MANE Select ENSP00000320885.3:p.Arg191Pro
ENST00000621856.2:c.569G>C ENSP00000482496.2:p.Arg190Pro
ENST00000642281.1:c.456G>C
ENST00000642455.1:c.569G>C ENSP00000493827.1:p.Arg190Pro
ENST00000642751.1:c.442G>C
ENST00000642999.1:c.314G>C ENSP00000496589.1:p.Arg105Pro
ENST00000643334.1:c.157G>C
ENST00000644408.1:c.448G>C
ENST00000644954.1:c.314G>C ENSP00000494312.1:p.Arg105Pro
ENST00000645400.1:c.528G>C ENSP00000496306.1:n.528G>C
ENST00000645671.1:c.37-9205G>C
ENST00000646082.1:c.406G>C
ENST00000646571.1:c.572G>C ENSP00000495015.1:p.Arg191Pro
ENST00000647007.1:n.269G>C
ENST00000647133.1:c.147G>C
ENST00000315285.7:c.572G>C ENSP00000320885.3:p.Arg191Pro
ENST00000345662.5:c.572G>C ENSP00000340817.1:p.Arg191Pro
ENST00000615843.4:c.572G>C ENSP00000480893.1:p.Arg191Pro
ENST00000621856.1:c.314G>C ENSP00000482496.1:p.Arg105Pro
NM_014946.3:c.572G>C , LRG_714t1:c.572G>C NP_055761.2:p.Arg191Pro
NM_199436.1:c.572G>C NP_955468.1:p.Arg191Pro
XM_005264516.3:c.569G>C XP_005264573.1:p.Arg190Pro
XM_011533067.1:c.572G>C XP_011531369.1:p.Arg191Pro
NM_001363823.1:c.569G>C NP_001350752.1:p.Arg190Pro
NM_001363875.1:c.569G>C NP_001350804.1:p.Arg190Pro
XM_005264516.5:c.569G>C XP_005264573.1:p.Arg190Pro
XM_011533067.2:c.572G>C XP_011531369.1:p.Arg191Pro
XM_017004778.2:c.572G>C XP_016860267.1:p.Arg191Pro
NM_001363823.2:c.569G>C NP_001350752.1:p.Arg190Pro
NM_001363875.2:c.569G>C NP_001350804.1:p.Arg190Pro
NM_001377959.1:c.572G>C NP_001364888.1:p.Arg191Pro
NM_014946.4:c.572G>C MANE Select NP_055761.2:p.Arg191Pro
NM_199436.2:c.572G>C NP_955468.1:p.Arg191Pro