Canonical Allele Identifier: CA2699030253

Gene: SPAST

Linked Data

• dbSNP Id: rs2148754188

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32137014_32137017dup , CM000664.2:g.32137014_32137017dup	GRCh38
NC_000002.11:g.32362083_32362086dup , CM000664.1:g.32362083_32362086dup	GRCh37
NC_000002.10:g.32215587_32215590dup	NCBI36
NG_008730.1:g.78404_78407dup , LRG_714:g.78404_78407dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*1073+46_*1073+49dup	ENSP00000515816.1:n.*1073+46_*1073+49dup
ENST00000315285.9:c.1413+46_1413+49dup MANE Select	ENSP00000320885.3:n.1413+46_1413+49dup
ENST00000621856.2:c.1410+46_1410+49dup	ENSP00000482496.2:n.1410+46_1410+49dup
ENST00000642281.1:c.1150+46_1150+49dup
ENST00000642455.1:c.1314+46_1314+49dup	ENSP00000493827.1:n.1314+46_1314+49dup
ENST00000642751.1:c.1187+46_1187+49dup
ENST00000642999.1:c.1155+46_1155+49dup	ENSP00000496589.1:n.1155+46_1155+49dup
ENST00000643327.1:c.481-95_481-92dup
ENST00000643334.1:c.993+46_993+49dup
ENST00000644408.1:c.1289+46_1289+49dup
ENST00000644954.1:c.1059+46_1059+49dup	ENSP00000494312.1:n.1059+46_1059+49dup
ENST00000645159.1:n.2150+46_2150+49dup
ENST00000645671.1:c.863+46_863+49dup
ENST00000645730.1:c.593-95_593-92dup
ENST00000646082.1:c.1059+46_1059+49dup
ENST00000646571.1:c.1317+46_1317+49dup	ENSP00000495015.1:n.1317+46_1317+49dup
ENST00000647007.1:n.1105+46_1105+49dup
ENST00000647133.1:c.913+46_913+49dup
ENST00000315285.7:c.1413+46_1413+49dup	ENSP00000320885.3:n.1413+46_1413+49dup
ENST00000345662.5:c.1317+46_1317+49dup	ENSP00000340817.1:n.1317+46_1317+49dup
ENST00000615843.4:c.1413+46_1413+49dup	ENSP00000480893.1:n.1413+46_1413+49dup
ENST00000621856.1:c.1155+46_1155+49dup	ENSP00000482496.1:n.1155+46_1155+49dup
NM_014946.3:c.1413+46_1413+49dup , LRG_714t1:c.1413+46_1413+49dup	NP_055761.2:n.1413+46_1413+49dup
NM_199436.1:c.1317+46_1317+49dup	NP_955468.1:n.1317+46_1317+49dup
XM_005264516.3:c.1410+46_1410+49dup	XP_005264573.1:n.1410+46_1410+49dup
XM_011533067.1:c.1413+46_1413+49dup	XP_011531369.1:n.1413+46_1413+49dup
NM_001363823.1:c.1410+46_1410+49dup	NP_001350752.1:n.1410+46_1410+49dup
NM_001363875.1:c.1314+46_1314+49dup	NP_001350804.1:n.1314+46_1314+49dup
XM_005264516.5:c.1410+46_1410+49dup	XP_005264573.1:n.1410+46_1410+49dup
XM_011533067.2:c.1413+46_1413+49dup	XP_011531369.1:n.1413+46_1413+49dup
XM_017004778.2:c.1317+46_1317+49dup	XP_016860267.1:n.1317+46_1317+49dup
NM_001363823.2:c.1410+46_1410+49dup	NP_001350752.1:n.1410+46_1410+49dup
NM_001363875.2:c.1314+46_1314+49dup	NP_001350804.1:n.1314+46_1314+49dup
NM_001377959.1:c.1317+46_1317+49dup	NP_001364888.1:n.1317+46_1317+49dup
NM_014946.4:c.1413+46_1413+49dup MANE Select	NP_055761.2:n.1413+46_1413+49dup
NM_199436.2:c.1317+46_1317+49dup	NP_955468.1:n.1317+46_1317+49dup