Canonical Allele Identifier: CA346502548

Gene: SPAST

Linked Data

• ClinVar Variation Id: 1335894
• ClinVar RCV Id: RCV001822087 ; RCV002473302
• dbSNP Id: rs2148754411
• MyVariant Identifiers: chr2:g.32362257G>C (hg19) ; chr2:g.32137188G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32137188G>C , CM000664.2:g.32137188G>C	GRCh38
NC_000002.11:g.32362257G>C , CM000664.1:g.32362257G>C	GRCh37
NC_000002.10:g.32215761G>C	NCBI36
NG_008730.1:g.78578G>C , LRG_714:g.78578G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*1153G>C	ENSP00000515816.1:n.*1153G>C
ENST00000315285.9:c.1493G>C MANE Select	ENSP00000320885.3:p.Arg498Thr
ENST00000621856.2:c.1490G>C	ENSP00000482496.2:p.Arg497Thr
ENST00000642281.1:c.1230G>C
ENST00000642455.1:c.1394G>C	ENSP00000493827.1:p.Arg465Thr
ENST00000642751.1:c.1267G>C
ENST00000642999.1:c.1235G>C	ENSP00000496589.1:p.Arg412Thr
ENST00000643327.1:c.560G>C
ENST00000643334.1:c.1073G>C
ENST00000644408.1:c.1369G>C
ENST00000644954.1:c.1139G>C	ENSP00000494312.1:p.Arg380Thr
ENST00000645159.1:n.2230G>C
ENST00000645671.1:c.943G>C
ENST00000645730.1:c.672G>C
ENST00000646082.1:c.1139G>C
ENST00000646571.1:c.1397G>C	ENSP00000495015.1:p.Arg466Thr
ENST00000647007.1:n.1185G>C
ENST00000647133.1:c.993G>C
ENST00000315285.7:c.1493G>C	ENSP00000320885.3:p.Arg498Thr
ENST00000345662.5:c.1397G>C	ENSP00000340817.1:p.Arg466Thr
ENST00000615843.4:c.1493G>C	ENSP00000480893.1:p.Arg498Thr
ENST00000621856.1:c.1235G>C	ENSP00000482496.1:p.Arg412Thr
NM_014946.3:c.1493G>C , LRG_714t1:c.1493G>C	NP_055761.2:p.Arg498Thr
NM_199436.1:c.1397G>C	NP_955468.1:p.Arg466Thr
XM_005264516.3:c.1490G>C	XP_005264573.1:p.Arg497Thr
XM_011533067.1:c.1493G>C	XP_011531369.1:p.Arg498Thr
NM_001363823.1:c.1490G>C	NP_001350752.1:p.Arg497Thr
NM_001363875.1:c.1394G>C	NP_001350804.1:p.Arg465Thr
XM_005264516.5:c.1490G>C	XP_005264573.1:p.Arg497Thr
XM_011533067.2:c.1493G>C	XP_011531369.1:p.Arg498Thr
XM_017004778.2:c.1397G>C	XP_016860267.1:p.Arg466Thr
NM_001363823.2:c.1490G>C	NP_001350752.1:p.Arg497Thr
NM_001363875.2:c.1394G>C	NP_001350804.1:p.Arg465Thr
NM_001377959.1:c.1397G>C	NP_001364888.1:p.Arg466Thr
NM_014946.4:c.1493G>C MANE Select	NP_055761.2:p.Arg498Thr
NM_199436.2:c.1397G>C	NP_955468.1:p.Arg466Thr