Canonical Allele Identifier: CA346502093

Gene: SPAST

Linked Data

• MyVariant Identifiers: chr2:g.32361684T>G (hg19) ; chr2:g.32136615T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32136615T>G , CM000664.2:g.32136615T>G	GRCh38
NC_000002.11:g.32361684T>G , CM000664.1:g.32361684T>G	GRCh37
NC_000002.10:g.32215188T>G	NCBI36
NG_008730.1:g.78005T>G , LRG_714:g.78005T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000704289.1:c.*958T>G	ENSP00000515816.1:n.*958T>G
ENST00000315285.9:c.1298T>G MANE Select	ENSP00000320885.3:p.Leu433Arg
ENST00000621856.2:c.1295T>G	ENSP00000482496.2:p.Leu432Arg
ENST00000642281.1:c.1035T>G
ENST00000642455.1:c.1199T>G	ENSP00000493827.1:p.Leu400Arg
ENST00000642751.1:c.1072T>G
ENST00000642999.1:c.1040T>G	ENSP00000496589.1:p.Leu347Arg
ENST00000643327.1:c.457T>G
ENST00000643334.1:c.878T>G
ENST00000644408.1:c.1174T>G
ENST00000644954.1:c.944T>G	ENSP00000494312.1:p.Leu315Arg
ENST00000645159.1:n.2035T>G
ENST00000645671.1:c.748T>G
ENST00000645730.1:c.593-494T>G
ENST00000646082.1:c.944T>G
ENST00000646571.1:c.1202T>G	ENSP00000495015.1:p.Leu401Arg
ENST00000647007.1:n.990T>G
ENST00000647133.1:c.798T>G
ENST00000315285.7:c.1298T>G	ENSP00000320885.3:p.Leu433Arg
ENST00000345662.5:c.1202T>G	ENSP00000340817.1:p.Leu401Arg
ENST00000615843.4:c.1298T>G	ENSP00000480893.1:p.Leu433Arg
ENST00000621856.1:c.1040T>G	ENSP00000482496.1:p.Leu347Arg
NM_014946.3:c.1298T>G , LRG_714t1:c.1298T>G	NP_055761.2:p.Leu433Arg
NM_199436.1:c.1202T>G	NP_955468.1:p.Leu401Arg
XM_005264516.3:c.1295T>G	XP_005264573.1:p.Leu432Arg
XM_011533067.1:c.1298T>G	XP_011531369.1:p.Leu433Arg
NM_001363823.1:c.1295T>G	NP_001350752.1:p.Leu432Arg
NM_001363875.1:c.1199T>G	NP_001350804.1:p.Leu400Arg
XM_005264516.5:c.1295T>G	XP_005264573.1:p.Leu432Arg
XM_011533067.2:c.1298T>G	XP_011531369.1:p.Leu433Arg
XM_017004778.2:c.1202T>G	XP_016860267.1:p.Leu401Arg
NM_001363823.2:c.1295T>G	NP_001350752.1:p.Leu432Arg
NM_001363875.2:c.1199T>G	NP_001350804.1:p.Leu400Arg
NM_001377959.1:c.1202T>G	NP_001364888.1:p.Leu401Arg
NM_014946.4:c.1298T>G MANE Select	NP_055761.2:p.Leu433Arg
NM_199436.2:c.1202T>G	NP_955468.1:p.Leu401Arg