Canonical Allele Identifier: CA1242505902
Gene: SPAST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32144990C= , CM000664.2:g.32144990C= GRCh38
NC_000002.11:g.32370059C= , CM000664.1:g.32370059C= GRCh37
NC_000002.10:g.32223563C= NCBI36
NG_008730.1:g.86380C= , LRG_714:g.86380C=

Transcript Alleles

HGVS Amino-acid Change
NM_014946.4:c.1670C= MANE Select NP_055761.2:p.Ala557=
ENST00000315285.9:c.1670C= MANE Select ENSP00000320885.3:p.Ala557=
NM_001363823.1:c.1667C= NP_001350752.1:p.Ala556=
NM_001363823.2:c.1667C= NP_001350752.1:p.Ala556=
NM_001363875.1:c.1571C= NP_001350804.1:p.Ala524=
NM_001363875.2:c.1571C= NP_001350804.1:p.Ala524=
NM_001377959.1:c.1520+1575C= NP_001364888.1:n.1520+1575C=
NM_014946.3:c.1670C= , LRG_714t1:c.1670C= NP_055761.2:p.Ala557=
NM_199436.1:c.1574C= NP_955468.1:p.Ala525=
NM_199436.2:c.1574C= NP_955468.1:p.Ala525=
ENST00000315285.7:c.1670C= ENSP00000320885.3:p.Ala557=
ENST00000345662.5:c.1574C= ENSP00000340817.1:p.Ala525=
ENST00000615843.4:c.1670C= ENSP00000480893.1:p.Ala557=
ENST00000621856.1:c.1412C= ENSP00000482496.1:p.Ala471=
ENST00000621856.2:c.1667C= ENSP00000482496.2:p.Ala556=
ENST00000642281.1:c.1407C=
ENST00000642455.1:c.1571C= ENSP00000493827.1:p.Ala524=
ENST00000642751.1:c.1390+1575C=
ENST00000642999.1:c.1412C= ENSP00000496589.1:p.Ala471=
ENST00000643334.1:c.1250C=
ENST00000644408.1:c.1546C=
ENST00000644954.1:c.1316C= ENSP00000494312.1:p.Ala439=
ENST00000645159.1:n.2407C=
ENST00000645671.1:c.1066+1575C=
ENST00000645730.1:c.849C=
ENST00000646082.1:c.1316C=
ENST00000646571.1:c.1574C= ENSP00000495015.1:p.Ala525=
ENST00000647007.1:n.1362C=
ENST00000647133.1:c.1170C=
ENST00000704289.1:c.*1330C= ENSP00000515816.1:n.*1330C=
XM_005264516.3:c.1667C= XP_005264573.1:p.Ala556=
XM_005264516.5:c.1667C= XP_005264573.1:p.Ala556=
XM_011533067.1:c.1616+1575C= XP_011531369.1:n.1616+1575C=
XM_011533067.2:c.1616+1575C= XP_011531369.1:n.1616+1575C=
XM_017004778.2:c.1520+1575C= XP_016860267.1:n.1520+1575C=