Canonical Allele Identifier: CA2586964736

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32136559_32136561delinsCT , CM000664.2:g.32136559_32136561delinsCT	GRCh38
NC_000002.11:g.32361628_32361630delinsCT , CM000664.1:g.32361628_32361630delinsCT	GRCh37
NC_000002.10:g.32215132_32215134delinsCT	NCBI36
NG_008730.1:g.77949_77951delinsCT , LRG_714:g.77949_77951delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*906-4_*906-2delinsCT	ENSP00000515816.1:n.*906-4_*906-2delinsCT
ENST00000315285.9:c.1246-4_1246-2delinsCT MANE Select	ENSP00000320885.3:n.1246-4_1246-2delinsCT
ENST00000621856.2:c.1243-4_1243-2delinsCT	ENSP00000482496.2:n.1243-4_1243-2delinsCT
ENST00000642281.1:c.983-4_983-2delinsCT
ENST00000642455.1:c.1147-4_1147-2delinsCT	ENSP00000493827.1:n.1147-4_1147-2delinsCT
ENST00000642751.1:c.1020-4_1020-2delinsCT
ENST00000642999.1:c.988-4_988-2delinsCT	ENSP00000496589.1:n.988-4_988-2delinsCT
ENST00000643327.1:c.405-4_405-2delinsCT
ENST00000643334.1:c.826-4_826-2delinsCT
ENST00000644408.1:c.1122-4_1122-2delinsCT
ENST00000644954.1:c.892-4_892-2delinsCT	ENSP00000494312.1:n.892-4_892-2delinsCT
ENST00000645159.1:n.1983-4_1983-2delinsCT
ENST00000645671.1:c.696-4_696-2delinsCT
ENST00000645730.1:c.593-550_593-548delinsCT
ENST00000646082.1:c.892-4_892-2delinsCT
ENST00000646571.1:c.1150-4_1150-2delinsCT	ENSP00000495015.1:n.1150-4_1150-2delinsCT
ENST00000647007.1:n.938-4_938-2delinsCT
ENST00000647133.1:c.746-4_746-2delinsCT
ENST00000315285.7:c.1246-4_1246-2delinsCT	ENSP00000320885.3:n.1246-4_1246-2delinsCT
ENST00000345662.5:c.1150-4_1150-2delinsCT	ENSP00000340817.1:n.1150-4_1150-2delinsCT
ENST00000615843.4:c.1246-4_1246-2delinsCT	ENSP00000480893.1:n.1246-4_1246-2delinsCT
ENST00000621856.1:c.988-4_988-2delinsCT	ENSP00000482496.1:n.988-4_988-2delinsCT
NM_014946.3:c.1246-4_1246-2delinsCT , LRG_714t1:c.1246-4_1246-2delinsCT	NP_055761.2:n.1246-4_1246-2delinsCT
NM_199436.1:c.1150-4_1150-2delinsCT	NP_955468.1:n.1150-4_1150-2delinsCT
XM_005264516.3:c.1243-4_1243-2delinsCT	XP_005264573.1:n.1243-4_1243-2delinsCT
XM_011533067.1:c.1246-4_1246-2delinsCT	XP_011531369.1:n.1246-4_1246-2delinsCT
NM_001363823.1:c.1243-4_1243-2delinsCT	NP_001350752.1:n.1243-4_1243-2delinsCT
NM_001363875.1:c.1147-4_1147-2delinsCT	NP_001350804.1:n.1147-4_1147-2delinsCT
XM_005264516.5:c.1243-4_1243-2delinsCT	XP_005264573.1:n.1243-4_1243-2delinsCT
XM_011533067.2:c.1246-4_1246-2delinsCT	XP_011531369.1:n.1246-4_1246-2delinsCT
XM_017004778.2:c.1150-4_1150-2delinsCT	XP_016860267.1:n.1150-4_1150-2delinsCT
NM_001363823.2:c.1243-4_1243-2delinsCT	NP_001350752.1:n.1243-4_1243-2delinsCT
NM_001363875.2:c.1147-4_1147-2delinsCT	NP_001350804.1:n.1147-4_1147-2delinsCT
NM_001377959.1:c.1150-4_1150-2delinsCT	NP_001364888.1:n.1150-4_1150-2delinsCT
NM_014946.4:c.1246-4_1246-2delinsCT MANE Select	NP_055761.2:n.1246-4_1246-2delinsCT
NM_199436.2:c.1150-4_1150-2delinsCT	NP_955468.1:n.1150-4_1150-2delinsCT