Canonical Allele Identifier: CA425448524

Gene: SPAST

Linked Data

• MyVariant Identifiers: chr2:g.32361677C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32136608C>A , CM000664.2:g.32136608C>A	GRCh38
NC_000002.11:g.32361677C>A , CM000664.1:g.32361677C>A	GRCh37
NC_000002.10:g.32215181C>A	NCBI36
NG_008730.1:g.77998C>A , LRG_714:g.77998C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000704289.1:c.*951C>A	ENSP00000515816.1:n.*951C>A
ENST00000315285.9:c.1291C>A MANE Select	ENSP00000320885.3:p.Arg431=
ENST00000621856.2:c.1288C>A	ENSP00000482496.2:p.Arg430=
ENST00000642281.1:c.1028C>A
ENST00000642455.1:c.1192C>A	ENSP00000493827.1:p.Arg398=
ENST00000642751.1:c.1065C>A
ENST00000642999.1:c.1033C>A	ENSP00000496589.1:p.Arg345=
ENST00000643327.1:c.450C>A
ENST00000643334.1:c.871C>A
ENST00000644408.1:c.1167C>A
ENST00000644954.1:c.937C>A	ENSP00000494312.1:p.Arg313=
ENST00000645159.1:n.2028C>A
ENST00000645671.1:c.741C>A
ENST00000645730.1:c.593-501C>A
ENST00000646082.1:c.937C>A
ENST00000646571.1:c.1195C>A	ENSP00000495015.1:p.Arg399=
ENST00000647007.1:n.983C>A
ENST00000647133.1:c.791C>A
ENST00000315285.7:c.1291C>A	ENSP00000320885.3:p.Arg431=
ENST00000345662.5:c.1195C>A	ENSP00000340817.1:p.Arg399=
ENST00000615843.4:c.1291C>A	ENSP00000480893.1:p.Arg431=
ENST00000621856.1:c.1033C>A	ENSP00000482496.1:p.Arg345=
NM_014946.3:c.1291C>A , LRG_714t1:c.1291C>A	NP_055761.2:p.Arg431=
NM_199436.1:c.1195C>A	NP_955468.1:p.Arg399=
XM_005264516.3:c.1288C>A	XP_005264573.1:p.Arg430=
XM_011533067.1:c.1291C>A	XP_011531369.1:p.Arg431=
NM_001363823.1:c.1288C>A	NP_001350752.1:p.Arg430=
NM_001363875.1:c.1192C>A	NP_001350804.1:p.Arg398=
XM_005264516.5:c.1288C>A	XP_005264573.1:p.Arg430=
XM_011533067.2:c.1291C>A	XP_011531369.1:p.Arg431=
XM_017004778.2:c.1195C>A	XP_016860267.1:p.Arg399=
NM_001363823.2:c.1288C>A	NP_001350752.1:p.Arg430=
NM_001363875.2:c.1192C>A	NP_001350804.1:p.Arg398=
NM_001377959.1:c.1195C>A	NP_001364888.1:p.Arg399=
NM_014946.4:c.1291C>A MANE Select	NP_055761.2:p.Arg431=
NM_199436.2:c.1195C>A	NP_955468.1:p.Arg399=