Canonical Allele Identifier: CA346504332
Gene: SPAST HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32147230A>G , CM000664.2:g.32147230A>G GRCh38
NC_000002.11:g.32372299A>G , CM000664.1:g.32372299A>G GRCh37
NC_000002.10:g.32225803A>G NCBI36
NG_008730.1:g.88620A>G , LRG_714:g.88620A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.*1360A>G ENSP00000515816.1:n.*1360A>G
ENST00000315285.9:c.1700A>G MANE Select ENSP00000320885.3:p.Glu567Gly
ENST00000621856.2:c.1697A>G ENSP00000482496.2:p.Glu566Gly
ENST00000642281.1:c.1437A>G
ENST00000642455.1:c.1601A>G ENSP00000493827.1:p.Glu534Gly
ENST00000642751.1:c.1403A>G
ENST00000642999.1:c.1442A>G ENSP00000496589.1:p.Glu481Gly
ENST00000643334.1:c.1280A>G
ENST00000644408.1:c.1599A>G
ENST00000644954.1:c.1346A>G ENSP00000494312.1:p.Glu449Gly
ENST00000645159.1:n.2437A>G
ENST00000645671.1:c.1079A>G
ENST00000645730.1:c.879A>G
ENST00000646082.1:c.1346A>G
ENST00000646571.1:c.1604A>G ENSP00000495015.1:p.Glu535Gly
ENST00000647007.1:n.1392A>G
ENST00000647133.1:c.1200A>G
ENST00000315285.7:c.1700A>G ENSP00000320885.3:p.Glu567Gly
ENST00000345662.5:c.1604A>G ENSP00000340817.1:p.Glu535Gly
ENST00000615843.4:c.1700A>G ENSP00000480893.1:p.Glu567Gly
ENST00000621856.1:c.1442A>G ENSP00000482496.1:p.Glu481Gly
NM_014946.3:c.1700A>G , LRG_714t1:c.1700A>G NP_055761.2:p.Glu567Gly
NM_199436.1:c.1604A>G NP_955468.1:p.Glu535Gly
XM_005264516.3:c.1697A>G XP_005264573.1:p.Glu566Gly
XM_011533067.1:c.1629A>G XP_011531369.1:p.Arg543=
NM_001363823.1:c.1697A>G NP_001350752.1:p.Glu566Gly
NM_001363875.1:c.1601A>G NP_001350804.1:p.Glu534Gly
XM_005264516.5:c.1697A>G XP_005264573.1:p.Glu566Gly
XM_011533067.2:c.1629A>G XP_011531369.1:p.Arg543=
XM_017004778.2:c.1533A>G XP_016860267.1:p.Arg511=
NM_001363823.2:c.1697A>G NP_001350752.1:p.Glu566Gly
NM_001363875.2:c.1601A>G NP_001350804.1:p.Glu534Gly
NM_001377959.1:c.1533A>G NP_001364888.1:p.Arg511=
NM_014946.4:c.1700A>G MANE Select NP_055761.2:p.Glu567Gly
NM_199436.2:c.1604A>G NP_955468.1:p.Glu535Gly