Canonical Allele Identifier: CA767786502

Gene: SPAST

Linked Data

• dbSNP Id: rs1313938817
• gnomAD v3: 2-32126684-C-CGGAA
• gnomAD v4: 2-32126684-C-CGGAA
• MyVariant Identifiers: chr2:g.32351753_32351754insGGAA (hg19) ; chr2:g.32126684_32126685insGGAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32126684_32126685insGGAA , CM000664.2:g.32126684_32126685insGGAA	GRCh38
NC_000002.11:g.32351753_32351754insGGAA , CM000664.1:g.32351753_32351754insGGAA	GRCh37
NC_000002.10:g.32205257_32205258insGGAA	NCBI36
NG_008730.1:g.68074_68075insGGAA , LRG_714:g.68074_68075insGGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*759-264_*759-263insGGAA	ENSP00000515816.1:n.*759-264_*759-263insGGAA
ENST00000315285.9:c.1099-264_1099-263insGGAA MANE Select	ENSP00000320885.3:n.1099-264_1099-263insGGAA
ENST00000621856.2:c.1096-264_1096-263insGGAA	ENSP00000482496.2:n.1096-264_1096-263insGGAA
ENST00000642281.1:c.983-9879_983-9878insGGAA
ENST00000642455.1:c.1000-264_1000-263insGGAA	ENSP00000493827.1:n.1000-264_1000-263insGGAA
ENST00000642751.1:c.873-264_873-263insGGAA
ENST00000642999.1:c.841-264_841-263insGGAA	ENSP00000496589.1:n.841-264_841-263insGGAA
ENST00000643327.1:c.258-264_258-263insGGAA
ENST00000643334.1:c.679-264_679-263insGGAA
ENST00000644408.1:c.975-264_975-263insGGAA
ENST00000644954.1:c.745-264_745-263insGGAA	ENSP00000494312.1:n.745-264_745-263insGGAA
ENST00000645159.1:n.187_188insGGAA
ENST00000645550.1:n.48_49insGGAA
ENST00000645671.1:c.549-264_549-263insGGAA
ENST00000645730.1:c.446-264_446-263insGGAA
ENST00000646082.1:c.745-264_745-263insGGAA
ENST00000646571.1:c.1003-264_1003-263insGGAA	ENSP00000495015.1:n.1003-264_1003-263insGGAA
ENST00000647007.1:n.791-264_791-263insGGAA
ENST00000647133.1:c.674-1724_674-1723insGGAA
ENST00000315285.7:c.1099-264_1099-263insGGAA	ENSP00000320885.3:n.1099-264_1099-263insGGAA
ENST00000345662.5:c.1003-264_1003-263insGGAA	ENSP00000340817.1:n.1003-264_1003-263insGGAA
ENST00000615843.4:c.1099-264_1099-263insGGAA	ENSP00000480893.1:n.1099-264_1099-263insGGAA
ENST00000621856.1:c.841-264_841-263insGGAA	ENSP00000482496.1:n.841-264_841-263insGGAA
NM_014946.3:c.1099-264_1099-263insGGAA , LRG_714t1:c.1099-264_1099-263insGGAA	NP_055761.2:n.1099-264_1099-263insGGAA
NM_199436.1:c.1003-264_1003-263insGGAA	NP_955468.1:n.1003-264_1003-263insGGAA
XM_005264516.3:c.1096-264_1096-263insGGAA	XP_005264573.1:n.1096-264_1096-263insGGAA
XM_011533067.1:c.1099-264_1099-263insGGAA	XP_011531369.1:n.1099-264_1099-263insGGAA
NM_001363823.1:c.1096-264_1096-263insGGAA	NP_001350752.1:n.1096-264_1096-263insGGAA
NM_001363875.1:c.1000-264_1000-263insGGAA	NP_001350804.1:n.1000-264_1000-263insGGAA
XM_005264516.5:c.1096-264_1096-263insGGAA	XP_005264573.1:n.1096-264_1096-263insGGAA
XM_011533067.2:c.1099-264_1099-263insGGAA	XP_011531369.1:n.1099-264_1099-263insGGAA
XM_017004778.2:c.1003-264_1003-263insGGAA	XP_016860267.1:n.1003-264_1003-263insGGAA
NM_001363823.2:c.1096-264_1096-263insGGAA	NP_001350752.1:n.1096-264_1096-263insGGAA
NM_001363875.2:c.1000-264_1000-263insGGAA	NP_001350804.1:n.1000-264_1000-263insGGAA
NM_001377959.1:c.1003-264_1003-263insGGAA	NP_001364888.1:n.1003-264_1003-263insGGAA
NM_014946.4:c.1099-264_1099-263insGGAA MANE Select	NP_055761.2:n.1099-264_1099-263insGGAA
NM_199436.2:c.1003-264_1003-263insGGAA	NP_955468.1:n.1003-264_1003-263insGGAA