Canonical Allele Identifier: CA1242505910
Gene: SPAST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32145004C= , CM000664.2:g.32145004C= GRCh38
NC_000002.11:g.32370073C= , CM000664.1:g.32370073C= GRCh37
NC_000002.10:g.32223577C= NCBI36
NG_008730.1:g.86394C= , LRG_714:g.86394C=

Transcript Alleles

HGVS Amino-acid Change
NM_014946.4:c.1684C= MANE Select NP_055761.2:p.Arg562=
ENST00000315285.9:c.1684C= MANE Select ENSP00000320885.3:p.Arg562=
NM_001363823.1:c.1681C= NP_001350752.1:p.Arg561=
NM_001363823.2:c.1681C= NP_001350752.1:p.Arg561=
NM_001363875.1:c.1585C= NP_001350804.1:p.Arg529=
NM_001363875.2:c.1585C= NP_001350804.1:p.Arg529=
NM_001377959.1:c.1520+1589C= NP_001364888.1:n.1520+1589C=
NM_014946.3:c.1684C= , LRG_714t1:c.1684C= NP_055761.2:p.Arg562=
NM_199436.1:c.1588C= NP_955468.1:p.Arg530=
NM_199436.2:c.1588C= NP_955468.1:p.Arg530=
ENST00000315285.7:c.1684C= ENSP00000320885.3:p.Arg562=
ENST00000345662.5:c.1588C= ENSP00000340817.1:p.Arg530=
ENST00000615843.4:c.1684C= ENSP00000480893.1:p.Arg562=
ENST00000621856.1:c.1426C= ENSP00000482496.1:p.Arg476=
ENST00000621856.2:c.1681C= ENSP00000482496.2:p.Arg561=
ENST00000642281.1:c.1421C=
ENST00000642455.1:c.1585C= ENSP00000493827.1:p.Arg529=
ENST00000642751.1:c.1390+1589C=
ENST00000642999.1:c.1426C= ENSP00000496589.1:p.Arg476=
ENST00000643334.1:c.1264C=
ENST00000644408.1:c.1560C=
ENST00000644954.1:c.1330C= ENSP00000494312.1:p.Arg444=
ENST00000645159.1:n.2421C=
ENST00000645671.1:c.1066+1589C=
ENST00000645730.1:c.863C=
ENST00000646082.1:c.1330C=
ENST00000646571.1:c.1588C= ENSP00000495015.1:p.Arg530=
ENST00000647007.1:n.1376C=
ENST00000647133.1:c.1184C=
ENST00000704289.1:c.*1344C= ENSP00000515816.1:n.*1344C=
XM_005264516.3:c.1681C= XP_005264573.1:p.Arg561=
XM_005264516.5:c.1681C= XP_005264573.1:p.Arg561=
XM_011533067.1:c.1616+1589C= XP_011531369.1:n.1616+1589C=
XM_011533067.2:c.1616+1589C= XP_011531369.1:n.1616+1589C=
XM_017004778.2:c.1520+1589C= XP_016860267.1:n.1520+1589C=