Canonical Allele Identifier: CA2503868855

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32126651_32126652insA , CM000664.2:g.32126651_32126652insA	GRCh38
NC_000002.11:g.32351720_32351721insA , CM000664.1:g.32351720_32351721insA	GRCh37
NC_000002.10:g.32205224_32205225insA	NCBI36
NG_008730.1:g.68041_68042insA , LRG_714:g.68041_68042insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*759-297_*759-296insA	ENSP00000515816.1:n.*759-297_*759-296insA
ENST00000315285.9:c.1099-297_1099-296insA MANE Select	ENSP00000320885.3:n.1099-297_1099-296insA
ENST00000621856.2:c.1096-297_1096-296insA	ENSP00000482496.2:n.1096-297_1096-296insA
ENST00000642281.1:c.983-9912_983-9911insA
ENST00000642455.1:c.1000-297_1000-296insA	ENSP00000493827.1:n.1000-297_1000-296insA
ENST00000642751.1:c.873-297_873-296insA
ENST00000642999.1:c.841-297_841-296insA	ENSP00000496589.1:n.841-297_841-296insA
ENST00000643327.1:c.258-297_258-296insA
ENST00000643334.1:c.679-297_679-296insA
ENST00000644408.1:c.975-297_975-296insA
ENST00000644954.1:c.745-297_745-296insA	ENSP00000494312.1:n.745-297_745-296insA
ENST00000645159.1:n.154_155insA
ENST00000645550.1:n.15_16insA
ENST00000645671.1:c.549-297_549-296insA
ENST00000645730.1:c.446-297_446-296insA
ENST00000646082.1:c.745-297_745-296insA
ENST00000646571.1:c.1003-297_1003-296insA	ENSP00000495015.1:n.1003-297_1003-296insA
ENST00000647007.1:n.791-297_791-296insA
ENST00000647133.1:c.674-1757_674-1756insA
ENST00000315285.7:c.1099-297_1099-296insA	ENSP00000320885.3:n.1099-297_1099-296insA
ENST00000345662.5:c.1003-297_1003-296insA	ENSP00000340817.1:n.1003-297_1003-296insA
ENST00000615843.4:c.1099-297_1099-296insA	ENSP00000480893.1:n.1099-297_1099-296insA
ENST00000621856.1:c.841-297_841-296insA	ENSP00000482496.1:n.841-297_841-296insA
NM_014946.3:c.1099-297_1099-296insA , LRG_714t1:c.1099-297_1099-296insA	NP_055761.2:n.1099-297_1099-296insA
NM_199436.1:c.1003-297_1003-296insA	NP_955468.1:n.1003-297_1003-296insA
XM_005264516.3:c.1096-297_1096-296insA	XP_005264573.1:n.1096-297_1096-296insA
XM_011533067.1:c.1099-297_1099-296insA	XP_011531369.1:n.1099-297_1099-296insA
NM_001363823.1:c.1096-297_1096-296insA	NP_001350752.1:n.1096-297_1096-296insA
NM_001363875.1:c.1000-297_1000-296insA	NP_001350804.1:n.1000-297_1000-296insA
XM_005264516.5:c.1096-297_1096-296insA	XP_005264573.1:n.1096-297_1096-296insA
XM_011533067.2:c.1099-297_1099-296insA	XP_011531369.1:n.1099-297_1099-296insA
XM_017004778.2:c.1003-297_1003-296insA	XP_016860267.1:n.1003-297_1003-296insA
NM_001363823.2:c.1096-297_1096-296insA	NP_001350752.1:n.1096-297_1096-296insA
NM_001363875.2:c.1000-297_1000-296insA	NP_001350804.1:n.1000-297_1000-296insA
NM_001377959.1:c.1003-297_1003-296insA	NP_001364888.1:n.1003-297_1003-296insA
NM_014946.4:c.1099-297_1099-296insA MANE Select	NP_055761.2:n.1099-297_1099-296insA
NM_199436.2:c.1003-297_1003-296insA	NP_955468.1:n.1003-297_1003-296insA