Canonical Allele Identifier: CA2586964645

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32126950_32126952del , CM000664.2:g.32126950_32126952del	GRCh38
NC_000002.11:g.32352019_32352021del , CM000664.1:g.32352019_32352021del	GRCh37
NC_000002.10:g.32205523_32205525del	NCBI36
NG_008730.1:g.68340_68342del , LRG_714:g.68340_68342del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*761_*763del
ENST00000315285.9:c.1101_1103del
ENST00000621856.2:c.1098_1100del
ENST00000642281.1:c.983-9613_983-9611del
ENST00000642455.1:c.1002_1004del
ENST00000642751.1:c.875_877del
ENST00000642999.1:c.843_845del
ENST00000643327.1:c.260_262del
ENST00000643334.1:c.681_683del
ENST00000644408.1:c.977_979del
ENST00000644954.1:c.747_749del
ENST00000645159.1:n.453_455del
ENST00000645550.1:n.314_316del
ENST00000645671.1:c.551_553del
ENST00000645730.1:c.448_450del
ENST00000646082.1:c.747_749del
ENST00000646571.1:c.1005_1007del
ENST00000647007.1:n.793_795del
ENST00000647133.1:c.674-1458_674-1456del
ENST00000315285.7:c.1101_1103del
ENST00000345662.5:c.1005_1007del
ENST00000615843.4:c.1101_1103del
ENST00000621856.1:c.843_845del
NM_014946.3:c.1101_1103del , LRG_714t1:c.1101_1103del
NM_199436.1:c.1005_1007del
XM_005264516.3:c.1098_1100del
XM_011533067.1:c.1101_1103del
NM_001363823.1:c.1098_1100del
NM_001363875.1:c.1002_1004del
XM_005264516.5:c.1098_1100del
XM_011533067.2:c.1101_1103del
XM_017004778.2:c.1005_1007del
NM_001363823.2:c.1098_1100del
NM_001363875.2:c.1002_1004del
NM_001377959.1:c.1005_1007del
NM_014946.4:c.1101_1103del
NM_199436.2:c.1005_1007del