Canonical Allele Identifier: CA2586964768

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32136967_32136968delinsAC , CM000664.2:g.32136967_32136968delinsAC	GRCh38
NC_000002.11:g.32362036_32362037delinsAC , CM000664.1:g.32362036_32362037delinsAC	GRCh37
NC_000002.10:g.32215540_32215541delinsAC	NCBI36
NG_008730.1:g.78357_78358delinsAC , LRG_714:g.78357_78358delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*1072_*1073delinsAC	ENSP00000515816.1:n.*1072_*1073delinsAC
ENST00000315285.9:c.1412_1413delinsAC MANE Select	ENSP00000320885.3:p.Gly471Asp
ENST00000621856.2:c.1409_1410delinsAC	ENSP00000482496.2:p.Gly470Asp
ENST00000642281.1:c.1149_1150delinsAC
ENST00000642455.1:c.1313_1314delinsAC	ENSP00000493827.1:p.Gly438Asp
ENST00000642751.1:c.1186_1187delinsAC
ENST00000642999.1:c.1154_1155delinsAC	ENSP00000496589.1:p.Gly385Asp
ENST00000643327.1:c.481-142_481-141delinsAC
ENST00000643334.1:c.992_993delinsAC
ENST00000644408.1:c.1288_1289delinsAC
ENST00000644954.1:c.1058_1059delinsAC	ENSP00000494312.1:p.Gly353Asp
ENST00000645159.1:n.2149_2150delinsAC
ENST00000645671.1:c.862_863delinsAC
ENST00000645730.1:c.593-142_593-141delinsAC
ENST00000646082.1:c.1058_1059delinsAC
ENST00000646571.1:c.1316_1317delinsAC	ENSP00000495015.1:p.Gly439Asp
ENST00000647007.1:n.1104_1105delinsAC
ENST00000647133.1:c.912_913delinsAC
ENST00000315285.7:c.1412_1413delinsAC	ENSP00000320885.3:p.Gly471Asp
ENST00000345662.5:c.1316_1317delinsAC	ENSP00000340817.1:p.Gly439Asp
ENST00000615843.4:c.1412_1413delinsAC	ENSP00000480893.1:p.Gly471Asp
ENST00000621856.1:c.1154_1155delinsAC	ENSP00000482496.1:p.Gly385Asp
NM_014946.3:c.1412_1413delinsAC , LRG_714t1:c.1412_1413delinsAC	NP_055761.2:p.Gly471Asp
NM_199436.1:c.1316_1317delinsAC	NP_955468.1:p.Gly439Asp
XM_005264516.3:c.1409_1410delinsAC	XP_005264573.1:p.Gly470Asp
XM_011533067.1:c.1412_1413delinsAC	XP_011531369.1:p.Gly471Asp
NM_001363823.1:c.1409_1410delinsAC	NP_001350752.1:p.Gly470Asp
NM_001363875.1:c.1313_1314delinsAC	NP_001350804.1:p.Gly438Asp
XM_005264516.5:c.1409_1410delinsAC	XP_005264573.1:p.Gly470Asp
XM_011533067.2:c.1412_1413delinsAC	XP_011531369.1:p.Gly471Asp
XM_017004778.2:c.1316_1317delinsAC	XP_016860267.1:p.Gly439Asp
NM_001363823.2:c.1409_1410delinsAC	NP_001350752.1:p.Gly470Asp
NM_001363875.2:c.1313_1314delinsAC	NP_001350804.1:p.Gly438Asp
NM_001377959.1:c.1316_1317delinsAC	NP_001364888.1:p.Gly439Asp
NM_014946.4:c.1412_1413delinsAC MANE Select	NP_055761.2:p.Gly471Asp
NM_199436.2:c.1316_1317delinsAC	NP_955468.1:p.Gly439Asp