Canonical Allele Identifier: CA346603589
Gene: SPAST HGNC NCBI

Linked Data

gnomAD v4: 2-32089596-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32089596C>A , CM000664.2:g.32089596C>A GRCh38
NC_000002.11:g.32314665C>A , CM000664.1:g.32314665C>A GRCh37
NC_000002.10:g.32168169C>A NCBI36
NG_008730.1:g.30986C>A , LRG_714:g.30986C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000704289.1:c.*237C>A ENSP00000515816.1:n.*237C>A
ENST00000315285.9:c.577C>A MANE Select ENSP00000320885.3:p.Gln193Lys
ENST00000621856.2:c.574C>A ENSP00000482496.2:p.Gln192Lys
ENST00000642281.1:c.461C>A
ENST00000642455.1:c.574C>A ENSP00000493827.1:p.Gln192Lys
ENST00000642751.1:c.447C>A
ENST00000642999.1:c.319C>A ENSP00000496589.1:p.Gln107Lys
ENST00000643334.1:c.162C>A
ENST00000644408.1:c.453C>A
ENST00000644954.1:c.319C>A ENSP00000494312.1:p.Gln107Lys
ENST00000645400.1:c.533C>A ENSP00000496306.1:n.533C>A
ENST00000645671.1:c.37-9200C>A
ENST00000646082.1:c.411C>A
ENST00000646571.1:c.577C>A ENSP00000495015.1:p.Gln193Lys
ENST00000647007.1:n.274C>A
ENST00000647133.1:c.152C>A
ENST00000315285.7:c.577C>A ENSP00000320885.3:p.Gln193Lys
ENST00000345662.5:c.577C>A ENSP00000340817.1:p.Gln193Lys
ENST00000615843.4:c.577C>A ENSP00000480893.1:p.Gln193Lys
ENST00000621856.1:c.319C>A ENSP00000482496.1:p.Gln107Lys
NM_014946.3:c.577C>A , LRG_714t1:c.577C>A NP_055761.2:p.Gln193Lys
NM_199436.1:c.577C>A NP_955468.1:p.Gln193Lys
XM_005264516.3:c.574C>A XP_005264573.1:p.Gln192Lys
XM_011533067.1:c.577C>A XP_011531369.1:p.Gln193Lys
NM_001363823.1:c.574C>A NP_001350752.1:p.Gln192Lys
NM_001363875.1:c.574C>A NP_001350804.1:p.Gln192Lys
XM_005264516.5:c.574C>A XP_005264573.1:p.Gln192Lys
XM_011533067.2:c.577C>A XP_011531369.1:p.Gln193Lys
XM_017004778.2:c.577C>A XP_016860267.1:p.Gln193Lys
NM_001363823.2:c.574C>A NP_001350752.1:p.Gln192Lys
NM_001363875.2:c.574C>A NP_001350804.1:p.Gln192Lys
NM_001377959.1:c.577C>A NP_001364888.1:p.Gln193Lys
NM_014946.4:c.577C>A MANE Select NP_055761.2:p.Gln193Lys
NM_199436.2:c.577C>A NP_955468.1:p.Gln193Lys