Canonical Allele Identifier: CA531500382

Gene: SPAST

Linked Data

• gnomAD v2: 2-32351728-TAA-T
• gnomAD v3: 2-32126659-TAA-T
• gnomAD v4: 2-32126659-TAA-T
• MyVariant Identifiers: chr2:g.32351729_32351730del (hg19) ; chr2:g.32126660_32126661del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32126660_32126661del , CM000664.2:g.32126660_32126661del	GRCh38
NC_000002.11:g.32351729_32351730del , CM000664.1:g.32351729_32351730del	GRCh37
NC_000002.10:g.32205233_32205234del	NCBI36
NG_008730.1:g.68050_68051del , LRG_714:g.68050_68051del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*759-288_*759-287del	ENSP00000515816.1:n.*759-288_*759-287del
ENST00000315285.9:c.1099-288_1099-287del MANE Select	ENSP00000320885.3:n.1099-288_1099-287del
ENST00000621856.2:c.1096-288_1096-287del	ENSP00000482496.2:n.1096-288_1096-287del
ENST00000642281.1:c.983-9903_983-9902del
ENST00000642455.1:c.1000-288_1000-287del	ENSP00000493827.1:n.1000-288_1000-287del
ENST00000642751.1:c.873-288_873-287del
ENST00000642999.1:c.841-288_841-287del	ENSP00000496589.1:n.841-288_841-287del
ENST00000643327.1:c.258-288_258-287del
ENST00000643334.1:c.679-288_679-287del
ENST00000644408.1:c.975-288_975-287del
ENST00000644954.1:c.745-288_745-287del	ENSP00000494312.1:n.745-288_745-287del
ENST00000645159.1:n.163_164del
ENST00000645550.1:n.24_25del
ENST00000645671.1:c.549-288_549-287del
ENST00000645730.1:c.446-288_446-287del
ENST00000646082.1:c.745-288_745-287del
ENST00000646571.1:c.1003-288_1003-287del	ENSP00000495015.1:n.1003-288_1003-287del
ENST00000647007.1:n.791-288_791-287del
ENST00000647133.1:c.674-1748_674-1747del
ENST00000315285.7:c.1099-288_1099-287del	ENSP00000320885.3:n.1099-288_1099-287del
ENST00000345662.5:c.1003-288_1003-287del	ENSP00000340817.1:n.1003-288_1003-287del
ENST00000615843.4:c.1099-288_1099-287del	ENSP00000480893.1:n.1099-288_1099-287del
ENST00000621856.1:c.841-288_841-287del	ENSP00000482496.1:n.841-288_841-287del
NM_014946.3:c.1099-288_1099-287del , LRG_714t1:c.1099-288_1099-287del	NP_055761.2:n.1099-288_1099-287del
NM_199436.1:c.1003-288_1003-287del	NP_955468.1:n.1003-288_1003-287del
XM_005264516.3:c.1096-288_1096-287del	XP_005264573.1:n.1096-288_1096-287del
XM_011533067.1:c.1099-288_1099-287del	XP_011531369.1:n.1099-288_1099-287del
NM_001363823.1:c.1096-288_1096-287del	NP_001350752.1:n.1096-288_1096-287del
NM_001363875.1:c.1000-288_1000-287del	NP_001350804.1:n.1000-288_1000-287del
XM_005264516.5:c.1096-288_1096-287del	XP_005264573.1:n.1096-288_1096-287del
XM_011533067.2:c.1099-288_1099-287del	XP_011531369.1:n.1099-288_1099-287del
XM_017004778.2:c.1003-288_1003-287del	XP_016860267.1:n.1003-288_1003-287del
NM_001363823.2:c.1096-288_1096-287del	NP_001350752.1:n.1096-288_1096-287del
NM_001363875.2:c.1000-288_1000-287del	NP_001350804.1:n.1000-288_1000-287del
NM_001377959.1:c.1003-288_1003-287del	NP_001364888.1:n.1003-288_1003-287del
NM_014946.4:c.1099-288_1099-287del MANE Select	NP_055761.2:n.1099-288_1099-287del
NM_199436.2:c.1003-288_1003-287del	NP_955468.1:n.1003-288_1003-287del