Canonical Allele Identifier: CA334385

Gene: SPAST

Linked Data

• ClinVar Variation Id: 188227
• ClinVar RCV Id: RCV000168164
• dbSNP Id: rs786204163
• MyVariant Identifiers: chr2:g.32362177G>C (hg19) ; chr2:g.32137108G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32137108G>C , CM000664.2:g.32137108G>C	GRCh38
NC_000002.11:g.32362177G>C , CM000664.1:g.32362177G>C	GRCh37
NC_000002.10:g.32215681G>C	NCBI36
NG_008730.1:g.78498G>C , LRG_714:g.78498G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*1074-1G>C	ENSP00000515816.1:n.*1074-1G>C
ENST00000315285.9:c.1414-1G>C MANE Select	ENSP00000320885.3:n.1414-1G>C
ENST00000621856.2:c.1411-1G>C	ENSP00000482496.2:n.1411-1G>C
ENST00000642281.1:c.1151-1G>C
ENST00000642455.1:c.1315-1G>C	ENSP00000493827.1:n.1315-1G>C
ENST00000642751.1:c.1188-1G>C
ENST00000642999.1:c.1156-1G>C	ENSP00000496589.1:n.1156-1G>C
ENST00000643327.1:c.481-1G>C
ENST00000643334.1:c.994-1G>C
ENST00000644408.1:c.1290-1G>C
ENST00000644954.1:c.1060-1G>C	ENSP00000494312.1:n.1060-1G>C
ENST00000645159.1:n.2151-1G>C
ENST00000645671.1:c.864-1G>C
ENST00000645730.1:c.593-1G>C
ENST00000646082.1:c.1060-1G>C
ENST00000646571.1:c.1318-1G>C	ENSP00000495015.1:n.1318-1G>C
ENST00000647007.1:n.1106-1G>C
ENST00000647133.1:c.914-1G>C
ENST00000315285.7:c.1414-1G>C	ENSP00000320885.3:n.1414-1G>C
ENST00000345662.5:c.1318-1G>C	ENSP00000340817.1:n.1318-1G>C
ENST00000615843.4:c.1414-1G>C	ENSP00000480893.1:n.1414-1G>C
ENST00000621856.1:c.1156-1G>C	ENSP00000482496.1:n.1156-1G>C
NM_014946.3:c.1414-1G>C , LRG_714t1:c.1414-1G>C	NP_055761.2:n.1414-1G>C
NM_199436.1:c.1318-1G>C	NP_955468.1:n.1318-1G>C
XM_005264516.3:c.1411-1G>C	XP_005264573.1:n.1411-1G>C
XM_011533067.1:c.1414-1G>C	XP_011531369.1:n.1414-1G>C
NM_001363823.1:c.1411-1G>C	NP_001350752.1:n.1411-1G>C
NM_001363875.1:c.1315-1G>C	NP_001350804.1:n.1315-1G>C
XM_005264516.5:c.1411-1G>C	XP_005264573.1:n.1411-1G>C
XM_011533067.2:c.1414-1G>C	XP_011531369.1:n.1414-1G>C
XM_017004778.2:c.1318-1G>C	XP_016860267.1:n.1318-1G>C
NM_001363823.2:c.1411-1G>C	NP_001350752.1:n.1411-1G>C
NM_001363875.2:c.1315-1G>C	NP_001350804.1:n.1315-1G>C
NM_001377959.1:c.1318-1G>C	NP_001364888.1:n.1318-1G>C
NM_014946.4:c.1414-1G>C MANE Select	NP_055761.2:n.1414-1G>C
NM_199436.2:c.1318-1G>C	NP_955468.1:n.1318-1G>C