Canonical Allele Identifier: CA337296

Gene: SPAST

Linked Data

• ClinVar Variation Id: 216111
• ClinVar RCV Id: RCV000197545
• dbSNP Id: rs757130394
• MyVariant Identifiers: chr2:g.32362181C>T (hg19) ; chr2:g.32137112C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32137112C>T , CM000664.2:g.32137112C>T	GRCh38
NC_000002.11:g.32362181C>T , CM000664.1:g.32362181C>T	GRCh37
NC_000002.10:g.32215685C>T	NCBI36
NG_008730.1:g.78502C>T , LRG_714:g.78502C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*1077C>T	ENSP00000515816.1:n.*1077C>T
ENST00000315285.9:c.1417C>T MANE Select	ENSP00000320885.3:p.Gln473Ter
ENST00000621856.2:c.1414C>T	ENSP00000482496.2:p.Gln472Ter
ENST00000642281.1:c.1154C>T
ENST00000642455.1:c.1318C>T	ENSP00000493827.1:p.Gln440Ter
ENST00000642751.1:c.1191C>T
ENST00000642999.1:c.1159C>T	ENSP00000496589.1:p.Gln387Ter
ENST00000643327.1:c.484C>T
ENST00000643334.1:c.997C>T
ENST00000644408.1:c.1293C>T
ENST00000644954.1:c.1063C>T	ENSP00000494312.1:p.Gln355Ter
ENST00000645159.1:n.2154C>T
ENST00000645671.1:c.867C>T
ENST00000645730.1:c.596C>T
ENST00000646082.1:c.1063C>T
ENST00000646571.1:c.1321C>T	ENSP00000495015.1:p.Gln441Ter
ENST00000647007.1:n.1109C>T
ENST00000647133.1:c.917C>T
ENST00000315285.7:c.1417C>T	ENSP00000320885.3:p.Gln473Ter
ENST00000345662.5:c.1321C>T	ENSP00000340817.1:p.Gln441Ter
ENST00000615843.4:c.1417C>T	ENSP00000480893.1:p.Gln473Ter
ENST00000621856.1:c.1159C>T	ENSP00000482496.1:p.Gln387Ter
NM_014946.3:c.1417C>T , LRG_714t1:c.1417C>T	NP_055761.2:p.Gln473Ter
NM_199436.1:c.1321C>T	NP_955468.1:p.Gln441Ter
XM_005264516.3:c.1414C>T	XP_005264573.1:p.Gln472Ter
XM_011533067.1:c.1417C>T	XP_011531369.1:p.Gln473Ter
NM_001363823.1:c.1414C>T	NP_001350752.1:p.Gln472Ter
NM_001363875.1:c.1318C>T	NP_001350804.1:p.Gln440Ter
XM_005264516.5:c.1414C>T	XP_005264573.1:p.Gln472Ter
XM_011533067.2:c.1417C>T	XP_011531369.1:p.Gln473Ter
XM_017004778.2:c.1321C>T	XP_016860267.1:p.Gln441Ter
NM_001363823.2:c.1414C>T	NP_001350752.1:p.Gln472Ter
NM_001363875.2:c.1318C>T	NP_001350804.1:p.Gln440Ter
NM_001377959.1:c.1321C>T	NP_001364888.1:p.Gln441Ter
NM_014946.4:c.1417C>T MANE Select	NP_055761.2:p.Gln473Ter
NM_199436.2:c.1321C>T	NP_955468.1:p.Gln441Ter