Canonical Allele Identifier: CA1242501954

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32137086_32137087delinsGA , CM000664.2:g.32137086_32137087delinsGA	GRCh38
NC_000002.11:g.32362155_32362156delinsGA , CM000664.1:g.32362155_32362156delinsGA	GRCh37
NC_000002.10:g.32215659_32215660delinsGA	NCBI36
NG_008730.1:g.78476_78477delinsGA , LRG_714:g.78476_78477delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*1074-23_*1074-22delinsGA	ENSP00000515816.1:n.*1074-23_*1074-22delinsGA
ENST00000315285.9:c.1414-23_1414-22delinsGA MANE Select	ENSP00000320885.3:n.1414-23_1414-22delinsGA
ENST00000621856.2:c.1411-23_1411-22delinsGA	ENSP00000482496.2:n.1411-23_1411-22delinsGA
ENST00000642281.1:c.1151-23_1151-22delinsGA
ENST00000642455.1:c.1315-23_1315-22delinsGA	ENSP00000493827.1:n.1315-23_1315-22delinsGA
ENST00000642751.1:c.1188-23_1188-22delinsGA
ENST00000642999.1:c.1156-23_1156-22delinsGA	ENSP00000496589.1:n.1156-23_1156-22delinsGA
ENST00000643327.1:c.481-23_481-22delinsGA
ENST00000643334.1:c.994-23_994-22delinsGA
ENST00000644408.1:c.1290-23_1290-22delinsGA
ENST00000644954.1:c.1060-23_1060-22delinsGA	ENSP00000494312.1:n.1060-23_1060-22delinsGA
ENST00000645159.1:n.2151-23_2151-22delinsGA
ENST00000645671.1:c.864-23_864-22delinsGA
ENST00000645730.1:c.593-23_593-22delinsGA
ENST00000646082.1:c.1060-23_1060-22delinsGA
ENST00000646571.1:c.1318-23_1318-22delinsGA	ENSP00000495015.1:n.1318-23_1318-22delinsGA
ENST00000647007.1:n.1106-23_1106-22delinsGA
ENST00000647133.1:c.914-23_914-22delinsGA
ENST00000315285.7:c.1414-23_1414-22delinsGA	ENSP00000320885.3:n.1414-23_1414-22delinsGA
ENST00000345662.5:c.1318-23_1318-22delinsGA	ENSP00000340817.1:n.1318-23_1318-22delinsGA
ENST00000615843.4:c.1414-23_1414-22delinsGA	ENSP00000480893.1:n.1414-23_1414-22delinsGA
ENST00000621856.1:c.1156-23_1156-22delinsGA	ENSP00000482496.1:n.1156-23_1156-22delinsGA
NM_014946.3:c.1414-23_1414-22delinsGA , LRG_714t1:c.1414-23_1414-22delinsGA	NP_055761.2:n.1414-23_1414-22delinsGA
NM_199436.1:c.1318-23_1318-22delinsGA	NP_955468.1:n.1318-23_1318-22delinsGA
XM_005264516.3:c.1411-23_1411-22delinsGA	XP_005264573.1:n.1411-23_1411-22delinsGA
XM_011533067.1:c.1414-23_1414-22delinsGA	XP_011531369.1:n.1414-23_1414-22delinsGA
NM_001363823.1:c.1411-23_1411-22delinsGA	NP_001350752.1:n.1411-23_1411-22delinsGA
NM_001363875.1:c.1315-23_1315-22delinsGA	NP_001350804.1:n.1315-23_1315-22delinsGA
XM_005264516.5:c.1411-23_1411-22delinsGA	XP_005264573.1:n.1411-23_1411-22delinsGA
XM_011533067.2:c.1414-23_1414-22delinsGA	XP_011531369.1:n.1414-23_1414-22delinsGA
XM_017004778.2:c.1318-23_1318-22delinsGA	XP_016860267.1:n.1318-23_1318-22delinsGA
NM_001363823.2:c.1411-23_1411-22delinsGA	NP_001350752.1:n.1411-23_1411-22delinsGA
NM_001363875.2:c.1315-23_1315-22delinsGA	NP_001350804.1:n.1315-23_1315-22delinsGA
NM_001377959.1:c.1318-23_1318-22delinsGA	NP_001364888.1:n.1318-23_1318-22delinsGA
NM_014946.4:c.1414-23_1414-22delinsGA MANE Select	NP_055761.2:n.1414-23_1414-22delinsGA
NM_199436.2:c.1318-23_1318-22delinsGA	NP_955468.1:n.1318-23_1318-22delinsGA