Canonical Allele Identifier: CA1242461831

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32064240_32064241delinsGA , CM000664.2:g.32064240_32064241delinsGA	GRCh38
NC_000002.11:g.32289309_32289310delinsGA , CM000664.1:g.32289309_32289310delinsGA	GRCh37
NC_000002.10:g.32142813_32142814delinsGA	NCBI36
NG_008730.1:g.5630_5631delinsGA , LRG_714:g.5630_5631delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.409_410delinsGA	ENSP00000515816.1:p.Glu137=
ENST00000315285.9:c.409_410delinsGA MANE Select	ENSP00000320885.3:p.Glu137=
ENST00000621856.2:c.409_410delinsGA	ENSP00000482496.2:p.Glu137=
ENST00000642281.1:c.293_294delinsGA
ENST00000642455.1:c.409_410delinsGA	ENSP00000493827.1:p.Glu137=
ENST00000642751.1:c.279_280delinsGA
ENST00000642999.1:c.151_152delinsGA	ENSP00000496589.1:p.Glu51=
ENST00000644408.1:c.285_286delinsGA
ENST00000644954.1:c.151_152delinsGA	ENSP00000494312.1:p.Glu51=
ENST00000645400.1:c.250_251delinsGA	ENSP00000496306.1:p.Glu84=
ENST00000645671.1:c.30_31delinsGA
ENST00000646082.1:c.243_244delinsGA
ENST00000646571.1:c.409_410delinsGA	ENSP00000495015.1:p.Glu137=
ENST00000315285.7:c.409_410delinsGA	ENSP00000320885.3:p.Glu137=
ENST00000345662.5:c.409_410delinsGA	ENSP00000340817.1:p.Glu137=
ENST00000615843.4:c.409_410delinsGA	ENSP00000480893.1:p.Glu137=
ENST00000621856.1:c.151_152delinsGA	ENSP00000482496.1:p.Glu51=
NM_014946.3:c.409_410delinsGA , LRG_714t1:c.409_410delinsGA	NP_055761.2:p.Glu137=
NM_199436.1:c.409_410delinsGA	NP_955468.1:p.Glu137=
XM_005264516.3:c.409_410delinsGA	XP_005264573.1:p.Glu137=
XM_011533067.1:c.409_410delinsGA	XP_011531369.1:p.Glu137=
NM_001363823.1:c.409_410delinsGA	NP_001350752.1:p.Glu137=
NM_001363875.1:c.409_410delinsGA	NP_001350804.1:p.Glu137=
XM_005264516.5:c.409_410delinsGA	XP_005264573.1:p.Glu137=
XM_011533067.2:c.409_410delinsGA	XP_011531369.1:p.Glu137=
XM_017004778.2:c.409_410delinsGA	XP_016860267.1:p.Glu137=
NM_001363823.2:c.409_410delinsGA	NP_001350752.1:p.Glu137=
NM_001363875.2:c.409_410delinsGA	NP_001350804.1:p.Glu137=
NM_001377959.1:c.409_410delinsGA	NP_001364888.1:p.Glu137=
NM_014946.4:c.409_410delinsGA MANE Select	NP_055761.2:p.Glu137=
NM_199436.2:c.409_410delinsGA	NP_955468.1:p.Glu137=