Canonical Allele Identifier: CA1242498153

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32128478_32128479delinsAC , CM000664.2:g.32128478_32128479delinsAC	GRCh38
NC_000002.11:g.32353547_32353548delinsAC , CM000664.1:g.32353547_32353548delinsAC	GRCh37
NC_000002.10:g.32207051_32207052delinsAC	NCBI36
NG_008730.1:g.69868_69869delinsAC , LRG_714:g.69868_69869delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000704289.1:c.*904_*905delinsAC	ENSP00000515816.1:n.*904_*905delinsAC
ENST00000315285.9:c.1244_1245delinsAC MANE Select	ENSP00000320885.3:p.Tyr415=
ENST00000621856.2:c.1241_1242delinsAC	ENSP00000482496.2:p.Tyr414=
ENST00000642281.1:c.983-8085_983-8084delinsAC
ENST00000642455.1:c.1145_1146delinsAC	ENSP00000493827.1:p.Tyr382=
ENST00000642751.1:c.1018_1019delinsAC
ENST00000642999.1:c.986_987delinsAC	ENSP00000496589.1:p.Tyr329=
ENST00000643327.1:c.403_404delinsAC
ENST00000643334.1:c.824_825delinsAC
ENST00000644408.1:c.1120_1121delinsAC
ENST00000644954.1:c.890_891delinsAC	ENSP00000494312.1:p.Tyr297=
ENST00000645159.1:n.1981_1982delinsAC
ENST00000645550.1:n.457_458delinsAC
ENST00000645671.1:c.694_695delinsAC
ENST00000645730.1:c.591_592delinsAC
ENST00000646082.1:c.890_891delinsAC
ENST00000646571.1:c.1148_1149delinsAC	ENSP00000495015.1:p.Tyr383=
ENST00000647007.1:n.936_937delinsAC
ENST00000647133.1:c.744_745delinsAC
ENST00000315285.7:c.1244_1245delinsAC	ENSP00000320885.3:p.Tyr415=
ENST00000345662.5:c.1148_1149delinsAC	ENSP00000340817.1:p.Tyr383=
ENST00000615843.4:c.1244_1245delinsAC	ENSP00000480893.1:p.Tyr415=
ENST00000621856.1:c.986_987delinsAC	ENSP00000482496.1:p.Tyr329=
NM_014946.3:c.1244_1245delinsAC , LRG_714t1:c.1244_1245delinsAC	NP_055761.2:p.Tyr415=
NM_199436.1:c.1148_1149delinsAC	NP_955468.1:p.Tyr383=
XM_005264516.3:c.1241_1242delinsAC	XP_005264573.1:p.Tyr414=
XM_011533067.1:c.1244_1245delinsAC	XP_011531369.1:p.Tyr415=
NM_001363823.1:c.1241_1242delinsAC	NP_001350752.1:p.Tyr414=
NM_001363875.1:c.1145_1146delinsAC	NP_001350804.1:p.Tyr382=
XM_005264516.5:c.1241_1242delinsAC	XP_005264573.1:p.Tyr414=
XM_011533067.2:c.1244_1245delinsAC	XP_011531369.1:p.Tyr415=
XM_017004778.2:c.1148_1149delinsAC	XP_016860267.1:p.Tyr383=
NM_001363823.2:c.1241_1242delinsAC	NP_001350752.1:p.Tyr414=
NM_001363875.2:c.1145_1146delinsAC	NP_001350804.1:p.Tyr382=
NM_001377959.1:c.1148_1149delinsAC	NP_001364888.1:p.Tyr383=
NM_014946.4:c.1244_1245delinsAC MANE Select	NP_055761.2:p.Tyr415=
NM_199436.2:c.1148_1149delinsAC	NP_955468.1:p.Tyr383=