Canonical Allele Identifier: CA2749393504

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32128294_32128295insAA , CM000664.2:g.32128294_32128295insAA	GRCh38
NC_000002.11:g.32353363_32353364insAA , CM000664.1:g.32353363_32353364insAA	GRCh37
NC_000002.10:g.32206867_32206868insAA	NCBI36
NG_008730.1:g.69684_69685insAA , LRG_714:g.69684_69685insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*834-114_*834-113insAA	ENSP00000515816.1:n.*834-114_*834-113insAA
ENST00000315285.9:c.1174-114_1174-113insAA MANE Select	ENSP00000320885.3:n.1174-114_1174-113insAA
ENST00000621856.2:c.1171-114_1171-113insAA	ENSP00000482496.2:n.1171-114_1171-113insAA
ENST00000642281.1:c.983-8269_983-8268insAA
ENST00000642455.1:c.1075-114_1075-113insAA	ENSP00000493827.1:n.1075-114_1075-113insAA
ENST00000642751.1:c.948-114_948-113insAA
ENST00000642999.1:c.916-114_916-113insAA	ENSP00000496589.1:n.916-114_916-113insAA
ENST00000643327.1:c.333-114_333-113insAA
ENST00000643334.1:c.754-114_754-113insAA
ENST00000644408.1:c.1050-114_1050-113insAA
ENST00000644954.1:c.820-114_820-113insAA	ENSP00000494312.1:n.820-114_820-113insAA
ENST00000645159.1:n.1797_1798insAA
ENST00000645550.1:n.387-114_387-113insAA
ENST00000645671.1:c.624-114_624-113insAA
ENST00000645730.1:c.521-114_521-113insAA
ENST00000646082.1:c.820-114_820-113insAA
ENST00000646571.1:c.1078-114_1078-113insAA	ENSP00000495015.1:n.1078-114_1078-113insAA
ENST00000647007.1:n.866-114_866-113insAA
ENST00000647133.1:c.674-114_674-113insAA
ENST00000315285.7:c.1174-114_1174-113insAA	ENSP00000320885.3:n.1174-114_1174-113insAA
ENST00000345662.5:c.1078-114_1078-113insAA	ENSP00000340817.1:n.1078-114_1078-113insAA
ENST00000615843.4:c.1174-114_1174-113insAA	ENSP00000480893.1:n.1174-114_1174-113insAA
ENST00000621856.1:c.916-114_916-113insAA	ENSP00000482496.1:n.916-114_916-113insAA
NM_014946.3:c.1174-114_1174-113insAA , LRG_714t1:c.1174-114_1174-113insAA	NP_055761.2:n.1174-114_1174-113insAA
NM_199436.1:c.1078-114_1078-113insAA	NP_955468.1:n.1078-114_1078-113insAA
XM_005264516.3:c.1171-114_1171-113insAA	XP_005264573.1:n.1171-114_1171-113insAA
XM_011533067.1:c.1174-114_1174-113insAA	XP_011531369.1:n.1174-114_1174-113insAA
NM_001363823.1:c.1171-114_1171-113insAA	NP_001350752.1:n.1171-114_1171-113insAA
NM_001363875.1:c.1075-114_1075-113insAA	NP_001350804.1:n.1075-114_1075-113insAA
XM_005264516.5:c.1171-114_1171-113insAA	XP_005264573.1:n.1171-114_1171-113insAA
XM_011533067.2:c.1174-114_1174-113insAA	XP_011531369.1:n.1174-114_1174-113insAA
XM_017004778.2:c.1078-114_1078-113insAA	XP_016860267.1:n.1078-114_1078-113insAA
NM_001363823.2:c.1171-114_1171-113insAA	NP_001350752.1:n.1171-114_1171-113insAA
NM_001363875.2:c.1075-114_1075-113insAA	NP_001350804.1:n.1075-114_1075-113insAA
NM_001377959.1:c.1078-114_1078-113insAA	NP_001364888.1:n.1078-114_1078-113insAA
NM_014946.4:c.1174-114_1174-113insAA MANE Select	NP_055761.2:n.1174-114_1174-113insAA
NM_199436.2:c.1078-114_1078-113insAA	NP_955468.1:n.1078-114_1078-113insAA