Canonical Allele Identifier: CA2532388627

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32126656_32126657insA , CM000664.2:g.32126656_32126657insA	GRCh38
NC_000002.11:g.32351725_32351726insA , CM000664.1:g.32351725_32351726insA	GRCh37
NC_000002.10:g.32205229_32205230insA	NCBI36
NG_008730.1:g.68046_68047insA , LRG_714:g.68046_68047insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*759-292_*759-291insA	ENSP00000515816.1:n.*759-292_*759-291insA
ENST00000315285.9:c.1099-292_1099-291insA MANE Select	ENSP00000320885.3:n.1099-292_1099-291insA
ENST00000621856.2:c.1096-292_1096-291insA	ENSP00000482496.2:n.1096-292_1096-291insA
ENST00000642281.1:c.983-9907_983-9906insA
ENST00000642455.1:c.1000-292_1000-291insA	ENSP00000493827.1:n.1000-292_1000-291insA
ENST00000642751.1:c.873-292_873-291insA
ENST00000642999.1:c.841-292_841-291insA	ENSP00000496589.1:n.841-292_841-291insA
ENST00000643327.1:c.258-292_258-291insA
ENST00000643334.1:c.679-292_679-291insA
ENST00000644408.1:c.975-292_975-291insA
ENST00000644954.1:c.745-292_745-291insA	ENSP00000494312.1:n.745-292_745-291insA
ENST00000645159.1:n.159_160insA
ENST00000645550.1:n.20_21insA
ENST00000645671.1:c.549-292_549-291insA
ENST00000645730.1:c.446-292_446-291insA
ENST00000646082.1:c.745-292_745-291insA
ENST00000646571.1:c.1003-292_1003-291insA	ENSP00000495015.1:n.1003-292_1003-291insA
ENST00000647007.1:n.791-292_791-291insA
ENST00000647133.1:c.674-1752_674-1751insA
ENST00000315285.7:c.1099-292_1099-291insA	ENSP00000320885.3:n.1099-292_1099-291insA
ENST00000345662.5:c.1003-292_1003-291insA	ENSP00000340817.1:n.1003-292_1003-291insA
ENST00000615843.4:c.1099-292_1099-291insA	ENSP00000480893.1:n.1099-292_1099-291insA
ENST00000621856.1:c.841-292_841-291insA	ENSP00000482496.1:n.841-292_841-291insA
NM_014946.3:c.1099-292_1099-291insA , LRG_714t1:c.1099-292_1099-291insA	NP_055761.2:n.1099-292_1099-291insA
NM_199436.1:c.1003-292_1003-291insA	NP_955468.1:n.1003-292_1003-291insA
XM_005264516.3:c.1096-292_1096-291insA	XP_005264573.1:n.1096-292_1096-291insA
XM_011533067.1:c.1099-292_1099-291insA	XP_011531369.1:n.1099-292_1099-291insA
NM_001363823.1:c.1096-292_1096-291insA	NP_001350752.1:n.1096-292_1096-291insA
NM_001363875.1:c.1000-292_1000-291insA	NP_001350804.1:n.1000-292_1000-291insA
XM_005264516.5:c.1096-292_1096-291insA	XP_005264573.1:n.1096-292_1096-291insA
XM_011533067.2:c.1099-292_1099-291insA	XP_011531369.1:n.1099-292_1099-291insA
XM_017004778.2:c.1003-292_1003-291insA	XP_016860267.1:n.1003-292_1003-291insA
NM_001363823.2:c.1096-292_1096-291insA	NP_001350752.1:n.1096-292_1096-291insA
NM_001363875.2:c.1000-292_1000-291insA	NP_001350804.1:n.1000-292_1000-291insA
NM_001377959.1:c.1003-292_1003-291insA	NP_001364888.1:n.1003-292_1003-291insA
NM_014946.4:c.1099-292_1099-291insA MANE Select	NP_055761.2:n.1099-292_1099-291insA
NM_199436.2:c.1003-292_1003-291insA	NP_955468.1:n.1003-292_1003-291insA