Canonical Allele Identifier: CA346499847

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32116199C>T , CM000664.2:g.32116199C>T	GRCh38
NC_000002.11:g.32341268C>T , CM000664.1:g.32341268C>T	GRCh37
NC_000002.10:g.32194772C>T	NCBI36
NG_008730.1:g.57589C>T , LRG_714:g.57589C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*745C>T	ENSP00000515816.1:n.*745C>T
ENST00000315285.9:c.1085C>T MANE Select	ENSP00000320885.3:p.Ser362Phe
ENST00000621856.2:c.1082C>T	ENSP00000482496.2:p.Ser361Phe
ENST00000642281.1:c.969C>T
ENST00000642455.1:c.986C>T	ENSP00000493827.1:p.Ser329Phe
ENST00000642751.1:c.859C>T
ENST00000642999.1:c.827C>T	ENSP00000496589.1:p.Ser276Phe
ENST00000643327.1:c.244C>T
ENST00000643334.1:c.665C>T
ENST00000644408.1:c.961C>T
ENST00000644954.1:c.731C>T	ENSP00000494312.1:p.Ser244Phe
ENST00000645671.1:c.535C>T
ENST00000645730.1:c.432C>T
ENST00000646082.1:c.731C>T
ENST00000646571.1:c.989C>T	ENSP00000495015.1:p.Ser330Phe
ENST00000647007.1:n.777C>T
ENST00000647133.1:c.660C>T
ENST00000315285.7:c.1085C>T	ENSP00000320885.3:p.Ser362Phe
ENST00000345662.5:c.989C>T	ENSP00000340817.1:p.Ser330Phe
ENST00000615843.4:c.1085C>T	ENSP00000480893.1:p.Ser362Phe
ENST00000621856.1:c.827C>T	ENSP00000482496.1:p.Ser276Phe
NM_014946.3:c.1085C>T , LRG_714t1:c.1085C>T	NP_055761.2:p.Ser362Phe
NM_199436.1:c.989C>T	NP_955468.1:p.Ser330Phe
XM_005264516.3:c.1082C>T	XP_005264573.1:p.Ser361Phe
XM_011533067.1:c.1085C>T	XP_011531369.1:p.Ser362Phe
NM_001363823.1:c.1082C>T	NP_001350752.1:p.Ser361Phe
NM_001363875.1:c.986C>T	NP_001350804.1:p.Ser329Phe
XM_005264516.5:c.1082C>T	XP_005264573.1:p.Ser361Phe
XM_011533067.2:c.1085C>T	XP_011531369.1:p.Ser362Phe
XM_017004778.2:c.989C>T	XP_016860267.1:p.Ser330Phe
NM_001363823.2:c.1082C>T	NP_001350752.1:p.Ser361Phe
NM_001363875.2:c.986C>T	NP_001350804.1:p.Ser329Phe
NM_001377959.1:c.989C>T	NP_001364888.1:p.Ser330Phe
NM_014946.4:c.1085C>T MANE Select	NP_055761.2:p.Ser362Phe
NM_199436.2:c.989C>T	NP_955468.1:p.Ser330Phe