Canonical Allele Identifier: CA2658526533

Gene: SPAST

Linked Data

• gnomAD v4: 2-32126781-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32126781_32126782insT , CM000664.2:g.32126781_32126782insT	GRCh38
NC_000002.11:g.32351850_32351851insT , CM000664.1:g.32351850_32351851insT	GRCh37
NC_000002.10:g.32205354_32205355insT	NCBI36
NG_008730.1:g.68171_68172insT , LRG_714:g.68171_68172insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*759-167_*759-166insT	ENSP00000515816.1:n.*759-167_*759-166insT
ENST00000315285.9:c.1099-167_1099-166insT MANE Select	ENSP00000320885.3:n.1099-167_1099-166insT
ENST00000621856.2:c.1096-167_1096-166insT	ENSP00000482496.2:n.1096-167_1096-166insT
ENST00000642281.1:c.983-9782_983-9781insT
ENST00000642455.1:c.1000-167_1000-166insT	ENSP00000493827.1:n.1000-167_1000-166insT
ENST00000642751.1:c.873-167_873-166insT
ENST00000642999.1:c.841-167_841-166insT	ENSP00000496589.1:n.841-167_841-166insT
ENST00000643327.1:c.258-167_258-166insT
ENST00000643334.1:c.679-167_679-166insT
ENST00000644408.1:c.975-167_975-166insT
ENST00000644954.1:c.745-167_745-166insT	ENSP00000494312.1:n.745-167_745-166insT
ENST00000645159.1:n.284_285insT
ENST00000645550.1:n.145_146insT
ENST00000645671.1:c.549-167_549-166insT
ENST00000645730.1:c.446-167_446-166insT
ENST00000646082.1:c.745-167_745-166insT
ENST00000646571.1:c.1003-167_1003-166insT	ENSP00000495015.1:n.1003-167_1003-166insT
ENST00000647007.1:n.791-167_791-166insT
ENST00000647133.1:c.674-1627_674-1626insT
ENST00000315285.7:c.1099-167_1099-166insT	ENSP00000320885.3:n.1099-167_1099-166insT
ENST00000345662.5:c.1003-167_1003-166insT	ENSP00000340817.1:n.1003-167_1003-166insT
ENST00000615843.4:c.1099-167_1099-166insT	ENSP00000480893.1:n.1099-167_1099-166insT
ENST00000621856.1:c.841-167_841-166insT	ENSP00000482496.1:n.841-167_841-166insT
NM_014946.3:c.1099-167_1099-166insT , LRG_714t1:c.1099-167_1099-166insT	NP_055761.2:n.1099-167_1099-166insT
NM_199436.1:c.1003-167_1003-166insT	NP_955468.1:n.1003-167_1003-166insT
XM_005264516.3:c.1096-167_1096-166insT	XP_005264573.1:n.1096-167_1096-166insT
XM_011533067.1:c.1099-167_1099-166insT	XP_011531369.1:n.1099-167_1099-166insT
NM_001363823.1:c.1096-167_1096-166insT	NP_001350752.1:n.1096-167_1096-166insT
NM_001363875.1:c.1000-167_1000-166insT	NP_001350804.1:n.1000-167_1000-166insT
XM_005264516.5:c.1096-167_1096-166insT	XP_005264573.1:n.1096-167_1096-166insT
XM_011533067.2:c.1099-167_1099-166insT	XP_011531369.1:n.1099-167_1099-166insT
XM_017004778.2:c.1003-167_1003-166insT	XP_016860267.1:n.1003-167_1003-166insT
NM_001363823.2:c.1096-167_1096-166insT	NP_001350752.1:n.1096-167_1096-166insT
NM_001363875.2:c.1000-167_1000-166insT	NP_001350804.1:n.1000-167_1000-166insT
NM_001377959.1:c.1003-167_1003-166insT	NP_001364888.1:n.1003-167_1003-166insT
NM_014946.4:c.1099-167_1099-166insT MANE Select	NP_055761.2:n.1099-167_1099-166insT
NM_199436.2:c.1003-167_1003-166insT	NP_955468.1:n.1003-167_1003-166insT