Canonical Allele Identifier: CA1242501307

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32136692_32136693delinsCA , CM000664.2:g.32136692_32136693delinsCA	GRCh38
NC_000002.11:g.32361761_32361762delinsCA , CM000664.1:g.32361761_32361762delinsCA	GRCh37
NC_000002.10:g.32215265_32215266delinsCA	NCBI36
NG_008730.1:g.78082_78083delinsCA , LRG_714:g.78082_78083delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*981+54_*981+55delinsCA	ENSP00000515816.1:n.*981+54_*981+55delinsCA
ENST00000315285.9:c.1321+54_1321+55delinsCA MANE Select	ENSP00000320885.3:n.1321+54_1321+55delinsCA
ENST00000621856.2:c.1318+54_1318+55delinsCA	ENSP00000482496.2:n.1318+54_1318+55delinsCA
ENST00000642281.1:c.1058+54_1058+55delinsCA
ENST00000642455.1:c.1222+54_1222+55delinsCA	ENSP00000493827.1:n.1222+54_1222+55delinsCA
ENST00000642751.1:c.1095+54_1095+55delinsCA
ENST00000642999.1:c.1063+54_1063+55delinsCA	ENSP00000496589.1:n.1063+54_1063+55delinsCA
ENST00000643327.1:c.480+54_480+55delinsCA
ENST00000643334.1:c.901+54_901+55delinsCA
ENST00000644408.1:c.1197+54_1197+55delinsCA
ENST00000644954.1:c.967+54_967+55delinsCA	ENSP00000494312.1:n.967+54_967+55delinsCA
ENST00000645159.1:n.2058+54_2058+55delinsCA
ENST00000645671.1:c.771+54_771+55delinsCA
ENST00000645730.1:c.593-417_593-416delinsCA
ENST00000646082.1:c.967+54_967+55delinsCA
ENST00000646571.1:c.1225+54_1225+55delinsCA	ENSP00000495015.1:n.1225+54_1225+55delinsCA
ENST00000647007.1:n.1013+54_1013+55delinsCA
ENST00000647133.1:c.821+54_821+55delinsCA
ENST00000315285.7:c.1321+54_1321+55delinsCA	ENSP00000320885.3:n.1321+54_1321+55delinsCA
ENST00000345662.5:c.1225+54_1225+55delinsCA	ENSP00000340817.1:n.1225+54_1225+55delinsCA
ENST00000615843.4:c.1321+54_1321+55delinsCA	ENSP00000480893.1:n.1321+54_1321+55delinsCA
ENST00000621856.1:c.1063+54_1063+55delinsCA	ENSP00000482496.1:n.1063+54_1063+55delinsCA
NM_014946.3:c.1321+54_1321+55delinsCA , LRG_714t1:c.1321+54_1321+55delinsCA	NP_055761.2:n.1321+54_1321+55delinsCA
NM_199436.1:c.1225+54_1225+55delinsCA	NP_955468.1:n.1225+54_1225+55delinsCA
XM_005264516.3:c.1318+54_1318+55delinsCA	XP_005264573.1:n.1318+54_1318+55delinsCA
XM_011533067.1:c.1321+54_1321+55delinsCA	XP_011531369.1:n.1321+54_1321+55delinsCA
NM_001363823.1:c.1318+54_1318+55delinsCA	NP_001350752.1:n.1318+54_1318+55delinsCA
NM_001363875.1:c.1222+54_1222+55delinsCA	NP_001350804.1:n.1222+54_1222+55delinsCA
XM_005264516.5:c.1318+54_1318+55delinsCA	XP_005264573.1:n.1318+54_1318+55delinsCA
XM_011533067.2:c.1321+54_1321+55delinsCA	XP_011531369.1:n.1321+54_1321+55delinsCA
XM_017004778.2:c.1225+54_1225+55delinsCA	XP_016860267.1:n.1225+54_1225+55delinsCA
NM_001363823.2:c.1318+54_1318+55delinsCA	NP_001350752.1:n.1318+54_1318+55delinsCA
NM_001363875.2:c.1222+54_1222+55delinsCA	NP_001350804.1:n.1222+54_1222+55delinsCA
NM_001377959.1:c.1225+54_1225+55delinsCA	NP_001364888.1:n.1225+54_1225+55delinsCA
NM_014946.4:c.1321+54_1321+55delinsCA MANE Select	NP_055761.2:n.1321+54_1321+55delinsCA
NM_199436.2:c.1225+54_1225+55delinsCA	NP_955468.1:n.1225+54_1225+55delinsCA