Canonical Allele Identifier: CA346501273

Gene: SPAST

Linked Data

• MyVariant Identifiers: chr2:g.32352056C>T (hg19) ; chr2:g.32126987C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32126987C>T , CM000664.2:g.32126987C>T	GRCh38
NC_000002.11:g.32352056C>T , CM000664.1:g.32352056C>T	GRCh37
NC_000002.10:g.32205560C>T	NCBI36
NG_008730.1:g.68377C>T , LRG_714:g.68377C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*798C>T	ENSP00000515816.1:n.*798C>T
ENST00000315285.9:c.1138C>T MANE Select	ENSP00000320885.3:p.Leu380Phe
ENST00000621856.2:c.1135C>T	ENSP00000482496.2:p.Leu379Phe
ENST00000642281.1:c.983-9576C>T
ENST00000642455.1:c.1039C>T	ENSP00000493827.1:p.Leu347Phe
ENST00000642751.1:c.912C>T
ENST00000642999.1:c.880C>T	ENSP00000496589.1:p.Leu294Phe
ENST00000643327.1:c.297C>T
ENST00000643334.1:c.718C>T
ENST00000644408.1:c.1014C>T
ENST00000644954.1:c.784C>T	ENSP00000494312.1:p.Leu262Phe
ENST00000645159.1:n.490C>T
ENST00000645550.1:n.351C>T
ENST00000645671.1:c.588C>T
ENST00000645730.1:c.485C>T
ENST00000646082.1:c.784C>T
ENST00000646571.1:c.1042C>T	ENSP00000495015.1:p.Leu348Phe
ENST00000647007.1:n.830C>T
ENST00000647133.1:c.674-1421C>T
ENST00000315285.7:c.1138C>T	ENSP00000320885.3:p.Leu380Phe
ENST00000345662.5:c.1042C>T	ENSP00000340817.1:p.Leu348Phe
ENST00000615843.4:c.1138C>T	ENSP00000480893.1:p.Leu380Phe
ENST00000621856.1:c.880C>T	ENSP00000482496.1:p.Leu294Phe
NM_014946.3:c.1138C>T , LRG_714t1:c.1138C>T	NP_055761.2:p.Leu380Phe
NM_199436.1:c.1042C>T	NP_955468.1:p.Leu348Phe
XM_005264516.3:c.1135C>T	XP_005264573.1:p.Leu379Phe
XM_011533067.1:c.1138C>T	XP_011531369.1:p.Leu380Phe
NM_001363823.1:c.1135C>T	NP_001350752.1:p.Leu379Phe
NM_001363875.1:c.1039C>T	NP_001350804.1:p.Leu347Phe
XM_005264516.5:c.1135C>T	XP_005264573.1:p.Leu379Phe
XM_011533067.2:c.1138C>T	XP_011531369.1:p.Leu380Phe
XM_017004778.2:c.1042C>T	XP_016860267.1:p.Leu348Phe
NM_001363823.2:c.1135C>T	NP_001350752.1:p.Leu379Phe
NM_001363875.2:c.1039C>T	NP_001350804.1:p.Leu347Phe
NM_001377959.1:c.1042C>T	NP_001364888.1:p.Leu348Phe
NM_014946.4:c.1138C>T MANE Select	NP_055761.2:p.Leu380Phe
NM_199436.2:c.1042C>T	NP_955468.1:p.Leu348Phe