Canonical Allele Identifier: CA1242498124

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32128436_32128437delinsCA , CM000664.2:g.32128436_32128437delinsCA	GRCh38
NC_000002.11:g.32353505_32353506delinsCA , CM000664.1:g.32353505_32353506delinsCA	GRCh37
NC_000002.10:g.32207009_32207010delinsCA	NCBI36
NG_008730.1:g.69826_69827delinsCA , LRG_714:g.69826_69827delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*862_*863delinsCA	ENSP00000515816.1:n.*862_*863delinsCA
ENST00000315285.9:c.1202_1203delinsCA MANE Select	ENSP00000320885.3:p.Ala401=
ENST00000621856.2:c.1199_1200delinsCA	ENSP00000482496.2:p.Ala400=
ENST00000642281.1:c.983-8127_983-8126delinsCA
ENST00000642455.1:c.1103_1104delinsCA	ENSP00000493827.1:p.Ala368=
ENST00000642751.1:c.976_977delinsCA
ENST00000642999.1:c.944_945delinsCA	ENSP00000496589.1:p.Ala315=
ENST00000643327.1:c.361_362delinsCA
ENST00000643334.1:c.782_783delinsCA
ENST00000644408.1:c.1078_1079delinsCA
ENST00000644954.1:c.848_849delinsCA	ENSP00000494312.1:p.Ala283=
ENST00000645159.1:n.1939_1940delinsCA
ENST00000645550.1:n.415_416delinsCA
ENST00000645671.1:c.652_653delinsCA
ENST00000645730.1:c.549_550delinsCA
ENST00000646082.1:c.848_849delinsCA
ENST00000646571.1:c.1106_1107delinsCA	ENSP00000495015.1:p.Ala369=
ENST00000647007.1:n.894_895delinsCA
ENST00000647133.1:c.702_703delinsCA
ENST00000315285.7:c.1202_1203delinsCA	ENSP00000320885.3:p.Ala401=
ENST00000345662.5:c.1106_1107delinsCA	ENSP00000340817.1:p.Ala369=
ENST00000615843.4:c.1202_1203delinsCA	ENSP00000480893.1:p.Ala401=
ENST00000621856.1:c.944_945delinsCA	ENSP00000482496.1:p.Ala315=
NM_014946.3:c.1202_1203delinsCA , LRG_714t1:c.1202_1203delinsCA	NP_055761.2:p.Ala401=
NM_199436.1:c.1106_1107delinsCA	NP_955468.1:p.Ala369=
XM_005264516.3:c.1199_1200delinsCA	XP_005264573.1:p.Ala400=
XM_011533067.1:c.1202_1203delinsCA	XP_011531369.1:p.Ala401=
NM_001363823.1:c.1199_1200delinsCA	NP_001350752.1:p.Ala400=
NM_001363875.1:c.1103_1104delinsCA	NP_001350804.1:p.Ala368=
XM_005264516.5:c.1199_1200delinsCA	XP_005264573.1:p.Ala400=
XM_011533067.2:c.1202_1203delinsCA	XP_011531369.1:p.Ala401=
XM_017004778.2:c.1106_1107delinsCA	XP_016860267.1:p.Ala369=
NM_001363823.2:c.1199_1200delinsCA	NP_001350752.1:p.Ala400=
NM_001363875.2:c.1103_1104delinsCA	NP_001350804.1:p.Ala368=
NM_001377959.1:c.1106_1107delinsCA	NP_001364888.1:p.Ala369=
NM_014946.4:c.1202_1203delinsCA MANE Select	NP_055761.2:p.Ala401=
NM_199436.2:c.1106_1107delinsCA	NP_955468.1:p.Ala369=