Canonical Allele Identifier: CA346502809

Gene: SPAST

Linked Data

• ClinVar Variation Id: 468568
• ClinVar RCV Id: RCV000544533 ; RCV000713466
• dbSNP Id: rs1218081251
• MyVariant Identifiers: chr2:g.32366971A>C (hg19) ; chr2:g.32141902A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32141902A>C , CM000664.2:g.32141902A>C	GRCh38
NC_000002.11:g.32366971A>C , CM000664.1:g.32366971A>C	GRCh37
NC_000002.10:g.32220475A>C	NCBI36
NG_008730.1:g.83292A>C , LRG_714:g.83292A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*1154-2A>C	ENSP00000515816.1:n.*1154-2A>C
ENST00000315285.9:c.1494-2A>C MANE Select	ENSP00000320885.3:n.1494-2A>C
ENST00000621856.2:c.1491-2A>C	ENSP00000482496.2:n.1491-2A>C
ENST00000642281.1:c.1231-2A>C
ENST00000642455.1:c.1395-2A>C	ENSP00000493827.1:n.1395-2A>C
ENST00000642751.1:c.1268-2A>C
ENST00000642999.1:c.1236-2A>C	ENSP00000496589.1:n.1236-2A>C
ENST00000643327.1:c.561-2A>C
ENST00000643334.1:c.1074-2A>C
ENST00000644408.1:c.1370-2A>C
ENST00000644954.1:c.1140-2A>C	ENSP00000494312.1:n.1140-2A>C
ENST00000645159.1:n.2231-2A>C
ENST00000645671.1:c.944-2A>C
ENST00000645730.1:c.673-2A>C
ENST00000646082.1:c.1140-2A>C
ENST00000646571.1:c.1398-2A>C	ENSP00000495015.1:n.1398-2A>C
ENST00000647007.1:n.1186-2A>C
ENST00000647133.1:c.994-2A>C
ENST00000315285.7:c.1494-2A>C	ENSP00000320885.3:n.1494-2A>C
ENST00000345662.5:c.1398-2A>C	ENSP00000340817.1:n.1398-2A>C
ENST00000615843.4:c.1494-2A>C	ENSP00000480893.1:n.1494-2A>C
ENST00000621856.1:c.1236-2A>C	ENSP00000482496.1:n.1236-2A>C
NM_014946.3:c.1494-2A>C , LRG_714t1:c.1494-2A>C	NP_055761.2:n.1494-2A>C
NM_199436.1:c.1398-2A>C	NP_955468.1:n.1398-2A>C
XM_005264516.3:c.1491-2A>C	XP_005264573.1:n.1491-2A>C
XM_011533067.1:c.1494-2A>C	XP_011531369.1:n.1494-2A>C
NM_001363823.1:c.1491-2A>C	NP_001350752.1:n.1491-2A>C
NM_001363875.1:c.1395-2A>C	NP_001350804.1:n.1395-2A>C
XM_005264516.5:c.1491-2A>C	XP_005264573.1:n.1491-2A>C
XM_011533067.2:c.1494-2A>C	XP_011531369.1:n.1494-2A>C
XM_017004778.2:c.1398-2A>C	XP_016860267.1:n.1398-2A>C
NM_001363823.2:c.1491-2A>C	NP_001350752.1:n.1491-2A>C
NM_001363875.2:c.1395-2A>C	NP_001350804.1:n.1395-2A>C
NM_001377959.1:c.1398-2A>C	NP_001364888.1:n.1398-2A>C
NM_014946.4:c.1494-2A>C MANE Select	NP_055761.2:n.1494-2A>C
NM_199436.2:c.1398-2A>C	NP_955468.1:n.1398-2A>C