Canonical Allele Identifier: CA2562227011

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32128509_32128510insGC , CM000664.2:g.32128509_32128510insGC	GRCh38
NC_000002.11:g.32353578_32353579insGC , CM000664.1:g.32353578_32353579insGC	GRCh37
NC_000002.10:g.32207082_32207083insGC	NCBI36
NG_008730.1:g.69899_69900insGC , LRG_714:g.69899_69900insGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000704289.1:c.*905+30_*905+31insGC	ENSP00000515816.1:n.*905+30_*905+31insGC
ENST00000315285.9:c.1245+30_1245+31insGC MANE Select	ENSP00000320885.3:n.1245+30_1245+31insGC
ENST00000621856.2:c.1242+30_1242+31insGC	ENSP00000482496.2:n.1242+30_1242+31insGC
ENST00000642281.1:c.983-8054_983-8053insGC
ENST00000642455.1:c.1146+30_1146+31insGC	ENSP00000493827.1:n.1146+30_1146+31insGC
ENST00000642751.1:c.1019+30_1019+31insGC
ENST00000642999.1:c.987+30_987+31insGC	ENSP00000496589.1:n.987+30_987+31insGC
ENST00000643327.1:c.404+30_404+31insGC
ENST00000643334.1:c.825+30_825+31insGC
ENST00000644408.1:c.1121+30_1121+31insGC
ENST00000644954.1:c.891+30_891+31insGC	ENSP00000494312.1:n.891+30_891+31insGC
ENST00000645159.1:n.1982+30_1982+31insGC
ENST00000645550.1:n.488_489insGC
ENST00000645671.1:c.695+30_695+31insGC
ENST00000645730.1:c.592+30_592+31insGC
ENST00000646082.1:c.891+30_891+31insGC
ENST00000646571.1:c.1149+30_1149+31insGC	ENSP00000495015.1:n.1149+30_1149+31insGC
ENST00000647007.1:n.937+30_937+31insGC
ENST00000647133.1:c.745+30_745+31insGC
ENST00000315285.7:c.1245+30_1245+31insGC	ENSP00000320885.3:n.1245+30_1245+31insGC
ENST00000345662.5:c.1149+30_1149+31insGC	ENSP00000340817.1:n.1149+30_1149+31insGC
ENST00000615843.4:c.1245+30_1245+31insGC	ENSP00000480893.1:n.1245+30_1245+31insGC
ENST00000621856.1:c.987+30_987+31insGC	ENSP00000482496.1:n.987+30_987+31insGC
NM_014946.3:c.1245+30_1245+31insGC , LRG_714t1:c.1245+30_1245+31insGC	NP_055761.2:n.1245+30_1245+31insGC
NM_199436.1:c.1149+30_1149+31insGC	NP_955468.1:n.1149+30_1149+31insGC
XM_005264516.3:c.1242+30_1242+31insGC	XP_005264573.1:n.1242+30_1242+31insGC
XM_011533067.1:c.1245+30_1245+31insGC	XP_011531369.1:n.1245+30_1245+31insGC
NM_001363823.1:c.1242+30_1242+31insGC	NP_001350752.1:n.1242+30_1242+31insGC
NM_001363875.1:c.1146+30_1146+31insGC	NP_001350804.1:n.1146+30_1146+31insGC
XM_005264516.5:c.1242+30_1242+31insGC	XP_005264573.1:n.1242+30_1242+31insGC
XM_011533067.2:c.1245+30_1245+31insGC	XP_011531369.1:n.1245+30_1245+31insGC
XM_017004778.2:c.1149+30_1149+31insGC	XP_016860267.1:n.1149+30_1149+31insGC
NM_001363823.2:c.1242+30_1242+31insGC	NP_001350752.1:n.1242+30_1242+31insGC
NM_001363875.2:c.1146+30_1146+31insGC	NP_001350804.1:n.1146+30_1146+31insGC
NM_001377959.1:c.1149+30_1149+31insGC	NP_001364888.1:n.1149+30_1149+31insGC
NM_014946.4:c.1245+30_1245+31insGC MANE Select	NP_055761.2:n.1245+30_1245+31insGC
NM_199436.2:c.1149+30_1149+31insGC	NP_955468.1:n.1149+30_1149+31insGC