Canonical Allele Identifier: CA333996

Gene: SPAST

Linked Data

• ClinVar Variation Id: 188083
• ClinVar RCV Id: RCV000167918
• dbSNP Id: rs786204057
• MyVariant Identifiers: chr2:g.32370026G>A (hg19) ; chr2:g.32144957G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32144957G>A , CM000664.2:g.32144957G>A	GRCh38
NC_000002.11:g.32370026G>A , CM000664.1:g.32370026G>A	GRCh37
NC_000002.10:g.32223530G>A	NCBI36
NG_008730.1:g.86347G>A , LRG_714:g.86347G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*1297G>A	ENSP00000515816.1:n.*1297G>A
ENST00000315285.9:c.1637G>A MANE Select	ENSP00000320885.3:p.Gly546Glu
ENST00000621856.2:c.1634G>A	ENSP00000482496.2:p.Gly545Glu
ENST00000642281.1:c.1374G>A
ENST00000642455.1:c.1538G>A	ENSP00000493827.1:p.Gly513Glu
ENST00000642751.1:c.1390+1542G>A
ENST00000642999.1:c.1379G>A	ENSP00000496589.1:p.Gly460Glu
ENST00000643334.1:c.1217G>A
ENST00000644408.1:c.1513G>A
ENST00000644954.1:c.1283G>A	ENSP00000494312.1:p.Gly428Glu
ENST00000645159.1:n.2374G>A
ENST00000645671.1:c.1066+1542G>A
ENST00000645730.1:c.816G>A
ENST00000646082.1:c.1283G>A
ENST00000646571.1:c.1541G>A	ENSP00000495015.1:p.Gly514Glu
ENST00000647007.1:n.1329G>A
ENST00000647133.1:c.1137G>A
ENST00000315285.7:c.1637G>A	ENSP00000320885.3:p.Gly546Glu
ENST00000345662.5:c.1541G>A	ENSP00000340817.1:p.Gly514Glu
ENST00000615843.4:c.1637G>A	ENSP00000480893.1:p.Gly546Glu
ENST00000621856.1:c.1379G>A	ENSP00000482496.1:p.Gly460Glu
NM_014946.3:c.1637G>A , LRG_714t1:c.1637G>A	NP_055761.2:p.Gly546Glu
NM_199436.1:c.1541G>A	NP_955468.1:p.Gly514Glu
XM_005264516.3:c.1634G>A	XP_005264573.1:p.Gly545Glu
XM_011533067.1:c.1616+1542G>A	XP_011531369.1:n.1616+1542G>A
NM_001363823.1:c.1634G>A	NP_001350752.1:p.Gly545Glu
NM_001363875.1:c.1538G>A	NP_001350804.1:p.Gly513Glu
XM_005264516.5:c.1634G>A	XP_005264573.1:p.Gly545Glu
XM_011533067.2:c.1616+1542G>A	XP_011531369.1:n.1616+1542G>A
XM_017004778.2:c.1520+1542G>A	XP_016860267.1:n.1520+1542G>A
NM_001363823.2:c.1634G>A	NP_001350752.1:p.Gly545Glu
NM_001363875.2:c.1538G>A	NP_001350804.1:p.Gly513Glu
NM_001377959.1:c.1520+1542G>A	NP_001364888.1:n.1520+1542G>A
NM_014946.4:c.1637G>A MANE Select	NP_055761.2:p.Gly546Glu
NM_199436.2:c.1541G>A	NP_955468.1:p.Gly514Glu