Canonical Allele Identifier: CA1242497323
Gene: SPAST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32126789T= , CM000664.2:g.32126789T= GRCh38
NC_000002.11:g.32351858T= , CM000664.1:g.32351858T= GRCh37
NC_000002.10:g.32205362T= NCBI36
NG_008730.1:g.68179T= , LRG_714:g.68179T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.*759-159T= ENSP00000515816.1:n.*759-159T=
ENST00000315285.9:c.1099-159T= MANE Select ENSP00000320885.3:n.1099-159T=
ENST00000621856.2:c.1096-159T= ENSP00000482496.2:n.1096-159T=
ENST00000642281.1:c.983-9774T=
ENST00000642455.1:c.1000-159T= ENSP00000493827.1:n.1000-159T=
ENST00000642751.1:c.873-159T=
ENST00000642999.1:c.841-159T= ENSP00000496589.1:n.841-159T=
ENST00000643327.1:c.258-159T=
ENST00000643334.1:c.679-159T=
ENST00000644408.1:c.975-159T=
ENST00000644954.1:c.745-159T= ENSP00000494312.1:n.745-159T=
ENST00000645159.1:n.292T=
ENST00000645550.1:n.153T=
ENST00000645671.1:c.549-159T=
ENST00000645730.1:c.446-159T=
ENST00000646082.1:c.745-159T=
ENST00000646571.1:c.1003-159T= ENSP00000495015.1:n.1003-159T=
ENST00000647007.1:n.791-159T=
ENST00000647133.1:c.674-1619T=
ENST00000315285.7:c.1099-159T= ENSP00000320885.3:n.1099-159T=
ENST00000345662.5:c.1003-159T= ENSP00000340817.1:n.1003-159T=
ENST00000615843.4:c.1099-159T= ENSP00000480893.1:n.1099-159T=
ENST00000621856.1:c.841-159T= ENSP00000482496.1:n.841-159T=
NM_014946.3:c.1099-159T= , LRG_714t1:c.1099-159T= NP_055761.2:n.1099-159T=
NM_199436.1:c.1003-159T= NP_955468.1:n.1003-159T=
XM_005264516.3:c.1096-159T= XP_005264573.1:n.1096-159T=
XM_011533067.1:c.1099-159T= XP_011531369.1:n.1099-159T=
NM_001363823.1:c.1096-159T= NP_001350752.1:n.1096-159T=
NM_001363875.1:c.1000-159T= NP_001350804.1:n.1000-159T=
XM_005264516.5:c.1096-159T= XP_005264573.1:n.1096-159T=
XM_011533067.2:c.1099-159T= XP_011531369.1:n.1099-159T=
XM_017004778.2:c.1003-159T= XP_016860267.1:n.1003-159T=
NM_001363823.2:c.1096-159T= NP_001350752.1:n.1096-159T=
NM_001363875.2:c.1000-159T= NP_001350804.1:n.1000-159T=
NM_001377959.1:c.1003-159T= NP_001364888.1:n.1003-159T=
NM_014946.4:c.1099-159T= MANE Select NP_055761.2:n.1099-159T=
NM_199436.2:c.1003-159T= NP_955468.1:n.1003-159T=