Canonical Allele Identifier: CA1242498151
Gene: SPAST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32128476A= , CM000664.2:g.32128476A= GRCh38
NC_000002.11:g.32353545A= , CM000664.1:g.32353545A= GRCh37
NC_000002.10:g.32207049A= NCBI36
NG_008730.1:g.69866A= , LRG_714:g.69866A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.*902A= ENSP00000515816.1:n.*902A=
ENST00000315285.9:c.1242A= MANE Select ENSP00000320885.3:p.Lys414=
ENST00000621856.2:c.1239A= ENSP00000482496.2:p.Lys413=
ENST00000642281.1:c.983-8087A=
ENST00000642455.1:c.1143A= ENSP00000493827.1:p.Lys381=
ENST00000642751.1:c.1016A=
ENST00000642999.1:c.984A= ENSP00000496589.1:p.Lys328=
ENST00000643327.1:c.401A=
ENST00000643334.1:c.822A=
ENST00000644408.1:c.1118A=
ENST00000644954.1:c.888A= ENSP00000494312.1:p.Lys296=
ENST00000645159.1:n.1979A=
ENST00000645550.1:n.455A=
ENST00000645671.1:c.692A=
ENST00000645730.1:c.589A=
ENST00000646082.1:c.888A=
ENST00000646571.1:c.1146A= ENSP00000495015.1:p.Lys382=
ENST00000647007.1:n.934A=
ENST00000647133.1:c.742A=
ENST00000315285.7:c.1242A= ENSP00000320885.3:p.Lys414=
ENST00000345662.5:c.1146A= ENSP00000340817.1:p.Lys382=
ENST00000615843.4:c.1242A= ENSP00000480893.1:p.Lys414=
ENST00000621856.1:c.984A= ENSP00000482496.1:p.Lys328=
NM_014946.3:c.1242A= , LRG_714t1:c.1242A= NP_055761.2:p.Lys414=
NM_199436.1:c.1146A= NP_955468.1:p.Lys382=
XM_005264516.3:c.1239A= XP_005264573.1:p.Lys413=
XM_011533067.1:c.1242A= XP_011531369.1:p.Lys414=
NM_001363823.1:c.1239A= NP_001350752.1:p.Lys413=
NM_001363875.1:c.1143A= NP_001350804.1:p.Lys381=
XM_005264516.5:c.1239A= XP_005264573.1:p.Lys413=
XM_011533067.2:c.1242A= XP_011531369.1:p.Lys414=
XM_017004778.2:c.1146A= XP_016860267.1:p.Lys382=
NM_001363823.2:c.1239A= NP_001350752.1:p.Lys413=
NM_001363875.2:c.1143A= NP_001350804.1:p.Lys381=
NM_001377959.1:c.1146A= NP_001364888.1:p.Lys382=
NM_014946.4:c.1242A= MANE Select NP_055761.2:p.Lys414=
NM_199436.2:c.1146A= NP_955468.1:p.Lys382=