Canonical Allele Identifier: CA2586964642

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32126946_32126948del , CM000664.2:g.32126946_32126948del	GRCh38
NC_000002.11:g.32352015_32352017del , CM000664.1:g.32352015_32352017del	GRCh37
NC_000002.10:g.32205519_32205521del	NCBI36
NG_008730.1:g.68336_68338del , LRG_714:g.68336_68338del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*759-2_*759del
ENST00000315285.9:c.1099-2_1099del
ENST00000621856.2:c.1096-2_1096del
ENST00000642281.1:c.983-9617_983-9615del
ENST00000642455.1:c.1000-2_1000del
ENST00000642751.1:c.873-2_873del
ENST00000642999.1:c.841-2_841del
ENST00000643327.1:c.258-2_258del
ENST00000643334.1:c.679-2_679del
ENST00000644408.1:c.975-2_975del
ENST00000644954.1:c.745-2_745del
ENST00000645159.1:n.449_451del
ENST00000645550.1:n.310_312del
ENST00000645671.1:c.549-2_549del
ENST00000645730.1:c.446-2_446del
ENST00000646082.1:c.745-2_745del
ENST00000646571.1:c.1003-2_1003del
ENST00000647007.1:n.791-2_791del
ENST00000647133.1:c.674-1462_674-1460del
ENST00000315285.7:c.1099-2_1099del
ENST00000345662.5:c.1003-2_1003del
ENST00000615843.4:c.1099-2_1099del
ENST00000621856.1:c.841-2_841del
NM_014946.3:c.1099-2_1099del , LRG_714t1:c.1099-2_1099del
NM_199436.1:c.1003-2_1003del
XM_005264516.3:c.1096-2_1096del
XM_011533067.1:c.1099-2_1099del
NM_001363823.1:c.1096-2_1096del
NM_001363875.1:c.1000-2_1000del
XM_005264516.5:c.1096-2_1096del
XM_011533067.2:c.1099-2_1099del
XM_017004778.2:c.1003-2_1003del
NM_001363823.2:c.1096-2_1096del
NM_001363875.2:c.1000-2_1000del
NM_001377959.1:c.1003-2_1003del
NM_014946.4:c.1099-2_1099del
NM_199436.2:c.1003-2_1003del