Canonical Allele Identifier: CA346501423

Gene: SPAST

Linked Data

• MyVariant Identifiers: chr2:g.32353505C>T (hg19) ; chr2:g.32128436C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32128436C>T , CM000664.2:g.32128436C>T	GRCh38
NC_000002.11:g.32353505C>T , CM000664.1:g.32353505C>T	GRCh37
NC_000002.10:g.32207009C>T	NCBI36
NG_008730.1:g.69826C>T , LRG_714:g.69826C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*862C>T	ENSP00000515816.1:n.*862C>T
ENST00000315285.9:c.1202C>T MANE Select	ENSP00000320885.3:p.Ala401Val
ENST00000621856.2:c.1199C>T	ENSP00000482496.2:p.Ala400Val
ENST00000642281.1:c.983-8127C>T
ENST00000642455.1:c.1103C>T	ENSP00000493827.1:p.Ala368Val
ENST00000642751.1:c.976C>T
ENST00000642999.1:c.944C>T	ENSP00000496589.1:p.Ala315Val
ENST00000643327.1:c.361C>T
ENST00000643334.1:c.782C>T
ENST00000644408.1:c.1078C>T
ENST00000644954.1:c.848C>T	ENSP00000494312.1:p.Ala283Val
ENST00000645159.1:n.1939C>T
ENST00000645550.1:n.415C>T
ENST00000645671.1:c.652C>T
ENST00000645730.1:c.549C>T
ENST00000646082.1:c.848C>T
ENST00000646571.1:c.1106C>T	ENSP00000495015.1:p.Ala369Val
ENST00000647007.1:n.894C>T
ENST00000647133.1:c.702C>T
ENST00000315285.7:c.1202C>T	ENSP00000320885.3:p.Ala401Val
ENST00000345662.5:c.1106C>T	ENSP00000340817.1:p.Ala369Val
ENST00000615843.4:c.1202C>T	ENSP00000480893.1:p.Ala401Val
ENST00000621856.1:c.944C>T	ENSP00000482496.1:p.Ala315Val
NM_014946.3:c.1202C>T , LRG_714t1:c.1202C>T	NP_055761.2:p.Ala401Val
NM_199436.1:c.1106C>T	NP_955468.1:p.Ala369Val
XM_005264516.3:c.1199C>T	XP_005264573.1:p.Ala400Val
XM_011533067.1:c.1202C>T	XP_011531369.1:p.Ala401Val
NM_001363823.1:c.1199C>T	NP_001350752.1:p.Ala400Val
NM_001363875.1:c.1103C>T	NP_001350804.1:p.Ala368Val
XM_005264516.5:c.1199C>T	XP_005264573.1:p.Ala400Val
XM_011533067.2:c.1202C>T	XP_011531369.1:p.Ala401Val
XM_017004778.2:c.1106C>T	XP_016860267.1:p.Ala369Val
NM_001363823.2:c.1199C>T	NP_001350752.1:p.Ala400Val
NM_001363875.2:c.1103C>T	NP_001350804.1:p.Ala368Val
NM_001377959.1:c.1106C>T	NP_001364888.1:p.Ala369Val
NM_014946.4:c.1202C>T MANE Select	NP_055761.2:p.Ala401Val
NM_199436.2:c.1106C>T	NP_955468.1:p.Ala369Val