Canonical Allele Identifier: CA346601485

Gene: SPAST

Linked Data

• ClinVar Variation Id: 835946
• ClinVar RCV Id: RCV001036951
• dbSNP Id: rs1356486929
• gnomAD v2: 2-32289052-A-G
• gnomAD v4: 2-32063983-A-G
• MyVariant Identifiers: chr2:g.32289052A>G (hg19) ; chr2:g.32063983A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32063983A>G , CM000664.2:g.32063983A>G	GRCh38
NC_000002.11:g.32289052A>G , CM000664.1:g.32289052A>G	GRCh37
NC_000002.10:g.32142556A>G	NCBI36
NG_008730.1:g.5373A>G , LRG_714:g.5373A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.152A>G	ENSP00000515816.1:p.Tyr51Cys
ENST00000315285.9:c.152A>G MANE Select	ENSP00000320885.3:p.Tyr51Cys
ENST00000621856.2:c.152A>G	ENSP00000482496.2:p.Tyr51Cys
ENST00000642281.1:c.36A>G
ENST00000642455.1:c.152A>G	ENSP00000493827.1:p.Tyr51Cys
ENST00000642751.1:c.22A>G
ENST00000642999.1:c.-107A>G	ENSP00000496589.1:n.-107A>G
ENST00000644408.1:c.28A>G
ENST00000644954.1:c.-107A>G	ENSP00000494312.1:n.-107A>G
ENST00000646571.1:c.152A>G	ENSP00000495015.1:p.Tyr51Cys
ENST00000315285.7:c.152A>G	ENSP00000320885.3:p.Tyr51Cys
ENST00000345662.5:c.152A>G	ENSP00000340817.1:p.Tyr51Cys
ENST00000615843.4:c.152A>G	ENSP00000480893.1:p.Tyr51Cys
ENST00000621856.1:c.-107A>G	ENSP00000482496.1:n.-107A>G
NM_014946.3:c.152A>G , LRG_714t1:c.152A>G	NP_055761.2:p.Tyr51Cys
NM_199436.1:c.152A>G	NP_955468.1:p.Tyr51Cys
XM_005264516.3:c.152A>G	XP_005264573.1:p.Tyr51Cys
XM_011533067.1:c.152A>G	XP_011531369.1:p.Tyr51Cys
NM_001363823.1:c.152A>G	NP_001350752.1:p.Tyr51Cys
NM_001363875.1:c.152A>G	NP_001350804.1:p.Tyr51Cys
XM_005264516.5:c.152A>G	XP_005264573.1:p.Tyr51Cys
XM_011533067.2:c.152A>G	XP_011531369.1:p.Tyr51Cys
XM_017004778.2:c.152A>G	XP_016860267.1:p.Tyr51Cys
NM_001363823.2:c.152A>G	NP_001350752.1:p.Tyr51Cys
NM_001363875.2:c.152A>G	NP_001350804.1:p.Tyr51Cys
NM_001377959.1:c.152A>G	NP_001364888.1:p.Tyr51Cys
NM_014946.4:c.152A>G MANE Select	NP_055761.2:p.Tyr51Cys
NM_199436.2:c.152A>G	NP_955468.1:p.Tyr51Cys