Canonical Allele Identifier: CA346501470

Gene: SPAST

Linked Data

• MyVariant Identifiers: chr2:g.32353526C>A (hg19) ; chr2:g.32128457C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32128457C>A , CM000664.2:g.32128457C>A	GRCh38
NC_000002.11:g.32353526C>A , CM000664.1:g.32353526C>A	GRCh37
NC_000002.10:g.32207030C>A	NCBI36
NG_008730.1:g.69847C>A , LRG_714:g.69847C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*883C>A	ENSP00000515816.1:n.*883C>A
ENST00000315285.9:c.1223C>A MANE Select	ENSP00000320885.3:p.Ala408Asp
ENST00000621856.2:c.1220C>A	ENSP00000482496.2:p.Ala407Asp
ENST00000642281.1:c.983-8106C>A
ENST00000642455.1:c.1124C>A	ENSP00000493827.1:p.Ala375Asp
ENST00000642751.1:c.997C>A
ENST00000642999.1:c.965C>A	ENSP00000496589.1:p.Ala322Asp
ENST00000643327.1:c.382C>A
ENST00000643334.1:c.803C>A
ENST00000644408.1:c.1099C>A
ENST00000644954.1:c.869C>A	ENSP00000494312.1:p.Ala290Asp
ENST00000645159.1:n.1960C>A
ENST00000645550.1:n.436C>A
ENST00000645671.1:c.673C>A
ENST00000645730.1:c.570C>A
ENST00000646082.1:c.869C>A
ENST00000646571.1:c.1127C>A	ENSP00000495015.1:p.Ala376Asp
ENST00000647007.1:n.915C>A
ENST00000647133.1:c.723C>A
ENST00000315285.7:c.1223C>A	ENSP00000320885.3:p.Ala408Asp
ENST00000345662.5:c.1127C>A	ENSP00000340817.1:p.Ala376Asp
ENST00000615843.4:c.1223C>A	ENSP00000480893.1:p.Ala408Asp
ENST00000621856.1:c.965C>A	ENSP00000482496.1:p.Ala322Asp
NM_014946.3:c.1223C>A , LRG_714t1:c.1223C>A	NP_055761.2:p.Ala408Asp
NM_199436.1:c.1127C>A	NP_955468.1:p.Ala376Asp
XM_005264516.3:c.1220C>A	XP_005264573.1:p.Ala407Asp
XM_011533067.1:c.1223C>A	XP_011531369.1:p.Ala408Asp
NM_001363823.1:c.1220C>A	NP_001350752.1:p.Ala407Asp
NM_001363875.1:c.1124C>A	NP_001350804.1:p.Ala375Asp
XM_005264516.5:c.1220C>A	XP_005264573.1:p.Ala407Asp
XM_011533067.2:c.1223C>A	XP_011531369.1:p.Ala408Asp
XM_017004778.2:c.1127C>A	XP_016860267.1:p.Ala376Asp
NM_001363823.2:c.1220C>A	NP_001350752.1:p.Ala407Asp
NM_001363875.2:c.1124C>A	NP_001350804.1:p.Ala375Asp
NM_001377959.1:c.1127C>A	NP_001364888.1:p.Ala376Asp
NM_014946.4:c.1223C>A MANE Select	NP_055761.2:p.Ala408Asp
NM_199436.2:c.1127C>A	NP_955468.1:p.Ala376Asp