Canonical Allele Identifier: CA425627752

Gene: SPAST

Linked Data

• ClinVar Variation Id: 1899250
• ClinVar RCV Id: RCV002575374
• MyVariant Identifiers: chr2:g.32289143C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32064074C>A , CM000664.2:g.32064074C>A	GRCh38
NC_000002.11:g.32289143C>A , CM000664.1:g.32289143C>A	GRCh37
NC_000002.10:g.32142647C>A	NCBI36
NG_008730.1:g.5464C>A , LRG_714:g.5464C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.243C>A	ENSP00000515816.1:p.Arg81=
ENST00000315285.9:c.243C>A MANE Select	ENSP00000320885.3:p.Arg81=
ENST00000621856.2:c.243C>A	ENSP00000482496.2:p.Arg81=
ENST00000642281.1:c.127C>A
ENST00000642455.1:c.243C>A	ENSP00000493827.1:p.Arg81=
ENST00000642751.1:c.113C>A
ENST00000642999.1:c.-16C>A	ENSP00000496589.1:n.-16C>A
ENST00000644408.1:c.119C>A
ENST00000644954.1:c.-16C>A	ENSP00000494312.1:n.-16C>A
ENST00000645400.1:c.84C>A	ENSP00000496306.1:p.Arg28=
ENST00000646082.1:c.77C>A
ENST00000646571.1:c.243C>A	ENSP00000495015.1:p.Arg81=
ENST00000315285.7:c.243C>A	ENSP00000320885.3:p.Arg81=
ENST00000345662.5:c.243C>A	ENSP00000340817.1:p.Arg81=
ENST00000615843.4:c.243C>A	ENSP00000480893.1:p.Arg81=
ENST00000621856.1:c.-16C>A	ENSP00000482496.1:n.-16C>A
NM_014946.3:c.243C>A , LRG_714t1:c.243C>A	NP_055761.2:p.Arg81=
NM_199436.1:c.243C>A	NP_955468.1:p.Arg81=
XM_005264516.3:c.243C>A	XP_005264573.1:p.Arg81=
XM_011533067.1:c.243C>A	XP_011531369.1:p.Arg81=
NM_001363823.1:c.243C>A	NP_001350752.1:p.Arg81=
NM_001363875.1:c.243C>A	NP_001350804.1:p.Arg81=
XM_005264516.5:c.243C>A	XP_005264573.1:p.Arg81=
XM_011533067.2:c.243C>A	XP_011531369.1:p.Arg81=
XM_017004778.2:c.243C>A	XP_016860267.1:p.Arg81=
NM_001363823.2:c.243C>A	NP_001350752.1:p.Arg81=
NM_001363875.2:c.243C>A	NP_001350804.1:p.Arg81=
NM_001377959.1:c.243C>A	NP_001364888.1:p.Arg81=
NM_014946.4:c.243C>A MANE Select	NP_055761.2:p.Arg81=
NM_199436.2:c.243C>A	NP_955468.1:p.Arg81=