Canonical Allele Identifier: CA346501478

Gene: SPAST

Linked Data

• ClinVar Variation Id: 963588
• ClinVar RCV Id: RCV001237635
• dbSNP Id: rs1679266894
• MyVariant Identifiers: chr2:g.32353531A>C (hg19) ; chr2:g.32128462A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32128462A>C , CM000664.2:g.32128462A>C	GRCh38
NC_000002.11:g.32353531A>C , CM000664.1:g.32353531A>C	GRCh37
NC_000002.10:g.32207035A>C	NCBI36
NG_008730.1:g.69852A>C , LRG_714:g.69852A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*888A>C	ENSP00000515816.1:n.*888A>C
ENST00000315285.9:c.1228A>C MANE Select	ENSP00000320885.3:p.Ser410Arg
ENST00000621856.2:c.1225A>C	ENSP00000482496.2:p.Ser409Arg
ENST00000642281.1:c.983-8101A>C
ENST00000642455.1:c.1129A>C	ENSP00000493827.1:p.Ser377Arg
ENST00000642751.1:c.1002A>C
ENST00000642999.1:c.970A>C	ENSP00000496589.1:p.Ser324Arg
ENST00000643327.1:c.387A>C
ENST00000643334.1:c.808A>C
ENST00000644408.1:c.1104A>C
ENST00000644954.1:c.874A>C	ENSP00000494312.1:p.Ser292Arg
ENST00000645159.1:n.1965A>C
ENST00000645550.1:n.441A>C
ENST00000645671.1:c.678A>C
ENST00000645730.1:c.575A>C
ENST00000646082.1:c.874A>C
ENST00000646571.1:c.1132A>C	ENSP00000495015.1:p.Ser378Arg
ENST00000647007.1:n.920A>C
ENST00000647133.1:c.728A>C
ENST00000315285.7:c.1228A>C	ENSP00000320885.3:p.Ser410Arg
ENST00000345662.5:c.1132A>C	ENSP00000340817.1:p.Ser378Arg
ENST00000615843.4:c.1228A>C	ENSP00000480893.1:p.Ser410Arg
ENST00000621856.1:c.970A>C	ENSP00000482496.1:p.Ser324Arg
NM_014946.3:c.1228A>C , LRG_714t1:c.1228A>C	NP_055761.2:p.Ser410Arg
NM_199436.1:c.1132A>C	NP_955468.1:p.Ser378Arg
XM_005264516.3:c.1225A>C	XP_005264573.1:p.Ser409Arg
XM_011533067.1:c.1228A>C	XP_011531369.1:p.Ser410Arg
NM_001363823.1:c.1225A>C	NP_001350752.1:p.Ser409Arg
NM_001363875.1:c.1129A>C	NP_001350804.1:p.Ser377Arg
XM_005264516.5:c.1225A>C	XP_005264573.1:p.Ser409Arg
XM_011533067.2:c.1228A>C	XP_011531369.1:p.Ser410Arg
XM_017004778.2:c.1132A>C	XP_016860267.1:p.Ser378Arg
NM_001363823.2:c.1225A>C	NP_001350752.1:p.Ser409Arg
NM_001363875.2:c.1129A>C	NP_001350804.1:p.Ser377Arg
NM_001377959.1:c.1132A>C	NP_001364888.1:p.Ser378Arg
NM_014946.4:c.1228A>C MANE Select	NP_055761.2:p.Ser410Arg
NM_199436.2:c.1132A>C	NP_955468.1:p.Ser378Arg