Canonical Allele Identifier: CA346501505

Gene: SPAST

Linked Data

• ClinVar Variation Id: 2760492
• ClinVar RCV Id: RCV003524742
• MyVariant Identifiers: chr2:g.32353543A>C (hg19) ; chr2:g.32128474A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32128474A>C , CM000664.2:g.32128474A>C	GRCh38
NC_000002.11:g.32353543A>C , CM000664.1:g.32353543A>C	GRCh37
NC_000002.10:g.32207047A>C	NCBI36
NG_008730.1:g.69864A>C , LRG_714:g.69864A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*900A>C	ENSP00000515816.1:n.*900A>C
ENST00000315285.9:c.1240A>C MANE Select	ENSP00000320885.3:p.Lys414Gln
ENST00000621856.2:c.1237A>C	ENSP00000482496.2:p.Lys413Gln
ENST00000642281.1:c.983-8089A>C
ENST00000642455.1:c.1141A>C	ENSP00000493827.1:p.Lys381Gln
ENST00000642751.1:c.1014A>C
ENST00000642999.1:c.982A>C	ENSP00000496589.1:p.Lys328Gln
ENST00000643327.1:c.399A>C
ENST00000643334.1:c.820A>C
ENST00000644408.1:c.1116A>C
ENST00000644954.1:c.886A>C	ENSP00000494312.1:p.Lys296Gln
ENST00000645159.1:n.1977A>C
ENST00000645550.1:n.453A>C
ENST00000645671.1:c.690A>C
ENST00000645730.1:c.587A>C
ENST00000646082.1:c.886A>C
ENST00000646571.1:c.1144A>C	ENSP00000495015.1:p.Lys382Gln
ENST00000647007.1:n.932A>C
ENST00000647133.1:c.740A>C
ENST00000315285.7:c.1240A>C	ENSP00000320885.3:p.Lys414Gln
ENST00000345662.5:c.1144A>C	ENSP00000340817.1:p.Lys382Gln
ENST00000615843.4:c.1240A>C	ENSP00000480893.1:p.Lys414Gln
ENST00000621856.1:c.982A>C	ENSP00000482496.1:p.Lys328Gln
NM_014946.3:c.1240A>C , LRG_714t1:c.1240A>C	NP_055761.2:p.Lys414Gln
NM_199436.1:c.1144A>C	NP_955468.1:p.Lys382Gln
XM_005264516.3:c.1237A>C	XP_005264573.1:p.Lys413Gln
XM_011533067.1:c.1240A>C	XP_011531369.1:p.Lys414Gln
NM_001363823.1:c.1237A>C	NP_001350752.1:p.Lys413Gln
NM_001363875.1:c.1141A>C	NP_001350804.1:p.Lys381Gln
XM_005264516.5:c.1237A>C	XP_005264573.1:p.Lys413Gln
XM_011533067.2:c.1240A>C	XP_011531369.1:p.Lys414Gln
XM_017004778.2:c.1144A>C	XP_016860267.1:p.Lys382Gln
NM_001363823.2:c.1237A>C	NP_001350752.1:p.Lys413Gln
NM_001363875.2:c.1141A>C	NP_001350804.1:p.Lys381Gln
NM_001377959.1:c.1144A>C	NP_001364888.1:p.Lys382Gln
NM_014946.4:c.1240A>C MANE Select	NP_055761.2:p.Lys414Gln
NM_199436.2:c.1144A>C	NP_955468.1:p.Lys382Gln