Canonical Allele Identifier: CA425451025

Gene: SPAST

Linked Data

• MyVariant Identifiers: chr2:g.32366976T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32141907T>A , CM000664.2:g.32141907T>A	GRCh38
NC_000002.11:g.32366976T>A , CM000664.1:g.32366976T>A	GRCh37
NC_000002.10:g.32220480T>A	NCBI36
NG_008730.1:g.83297T>A , LRG_714:g.83297T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000704289.1:c.*1157T>A	ENSP00000515816.1:n.*1157T>A
ENST00000315285.9:c.1497T>A MANE Select	ENSP00000320885.3:p.Arg499=
ENST00000621856.2:c.1494T>A	ENSP00000482496.2:p.Arg498=
ENST00000642281.1:c.1234T>A
ENST00000642455.1:c.1398T>A	ENSP00000493827.1:p.Arg466=
ENST00000642751.1:c.1271T>A
ENST00000642999.1:c.1239T>A	ENSP00000496589.1:p.Arg413=
ENST00000643327.1:c.564T>A
ENST00000643334.1:c.1077T>A
ENST00000644408.1:c.1373T>A
ENST00000644954.1:c.1143T>A	ENSP00000494312.1:p.Arg381=
ENST00000645159.1:n.2234T>A
ENST00000645671.1:c.947T>A
ENST00000645730.1:c.676T>A
ENST00000646082.1:c.1143T>A
ENST00000646571.1:c.1401T>A	ENSP00000495015.1:p.Arg467=
ENST00000647007.1:n.1189T>A
ENST00000647133.1:c.997T>A
ENST00000315285.7:c.1497T>A	ENSP00000320885.3:p.Arg499=
ENST00000345662.5:c.1401T>A	ENSP00000340817.1:p.Arg467=
ENST00000615843.4:c.1497T>A	ENSP00000480893.1:p.Arg499=
ENST00000621856.1:c.1239T>A	ENSP00000482496.1:p.Arg413=
NM_014946.3:c.1497T>A , LRG_714t1:c.1497T>A	NP_055761.2:p.Arg499=
NM_199436.1:c.1401T>A	NP_955468.1:p.Arg467=
XM_005264516.3:c.1494T>A	XP_005264573.1:p.Arg498=
XM_011533067.1:c.1497T>A	XP_011531369.1:p.Arg499=
NM_001363823.1:c.1494T>A	NP_001350752.1:p.Arg498=
NM_001363875.1:c.1398T>A	NP_001350804.1:p.Arg466=
XM_005264516.5:c.1494T>A	XP_005264573.1:p.Arg498=
XM_011533067.2:c.1497T>A	XP_011531369.1:p.Arg499=
XM_017004778.2:c.1401T>A	XP_016860267.1:p.Arg467=
NM_001363823.2:c.1494T>A	NP_001350752.1:p.Arg498=
NM_001363875.2:c.1398T>A	NP_001350804.1:p.Arg466=
NM_001377959.1:c.1401T>A	NP_001364888.1:p.Arg467=
NM_014946.4:c.1497T>A MANE Select	NP_055761.2:p.Arg499=
NM_199436.2:c.1401T>A	NP_955468.1:p.Arg467=