Canonical Allele Identifier: CA425449223

Gene: SPAST

Linked Data

• MyVariant Identifiers: chr2:g.32362252T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32137183T>A , CM000664.2:g.32137183T>A	GRCh38
NC_000002.11:g.32362252T>A , CM000664.1:g.32362252T>A	GRCh37
NC_000002.10:g.32215756T>A	NCBI36
NG_008730.1:g.78573T>A , LRG_714:g.78573T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*1148T>A	ENSP00000515816.1:n.*1148T>A
ENST00000315285.9:c.1488T>A MANE Select	ENSP00000320885.3:p.Val496=
ENST00000621856.2:c.1485T>A	ENSP00000482496.2:p.Val495=
ENST00000642281.1:c.1225T>A
ENST00000642455.1:c.1389T>A	ENSP00000493827.1:p.Val463=
ENST00000642751.1:c.1262T>A
ENST00000642999.1:c.1230T>A	ENSP00000496589.1:p.Val410=
ENST00000643327.1:c.555T>A
ENST00000643334.1:c.1068T>A
ENST00000644408.1:c.1364T>A
ENST00000644954.1:c.1134T>A	ENSP00000494312.1:p.Val378=
ENST00000645159.1:n.2225T>A
ENST00000645671.1:c.938T>A
ENST00000645730.1:c.667T>A
ENST00000646082.1:c.1134T>A
ENST00000646571.1:c.1392T>A	ENSP00000495015.1:p.Val464=
ENST00000647007.1:n.1180T>A
ENST00000647133.1:c.988T>A
ENST00000315285.7:c.1488T>A	ENSP00000320885.3:p.Val496=
ENST00000345662.5:c.1392T>A	ENSP00000340817.1:p.Val464=
ENST00000615843.4:c.1488T>A	ENSP00000480893.1:p.Val496=
ENST00000621856.1:c.1230T>A	ENSP00000482496.1:p.Val410=
NM_014946.3:c.1488T>A , LRG_714t1:c.1488T>A	NP_055761.2:p.Val496=
NM_199436.1:c.1392T>A	NP_955468.1:p.Val464=
XM_005264516.3:c.1485T>A	XP_005264573.1:p.Val495=
XM_011533067.1:c.1488T>A	XP_011531369.1:p.Val496=
NM_001363823.1:c.1485T>A	NP_001350752.1:p.Val495=
NM_001363875.1:c.1389T>A	NP_001350804.1:p.Val463=
XM_005264516.5:c.1485T>A	XP_005264573.1:p.Val495=
XM_011533067.2:c.1488T>A	XP_011531369.1:p.Val496=
XM_017004778.2:c.1392T>A	XP_016860267.1:p.Val464=
NM_001363823.2:c.1485T>A	NP_001350752.1:p.Val495=
NM_001363875.2:c.1389T>A	NP_001350804.1:p.Val463=
NM_001377959.1:c.1392T>A	NP_001364888.1:p.Val464=
NM_014946.4:c.1488T>A MANE Select	NP_055761.2:p.Val496=
NM_199436.2:c.1392T>A	NP_955468.1:p.Val464=