Canonical Allele Identifier: CA346501309

Gene: SPAST

Linked Data

• MyVariant Identifiers: chr2:g.32352072G>T (hg19) ; chr2:g.32127003G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32127003G>T , CM000664.2:g.32127003G>T	GRCh38
NC_000002.11:g.32352072G>T , CM000664.1:g.32352072G>T	GRCh37
NC_000002.10:g.32205576G>T	NCBI36
NG_008730.1:g.68393G>T , LRG_714:g.68393G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*814G>T	ENSP00000515816.1:n.*814G>T
ENST00000315285.9:c.1154G>T MANE Select	ENSP00000320885.3:p.Gly385Val
ENST00000621856.2:c.1151G>T	ENSP00000482496.2:p.Gly384Val
ENST00000642281.1:c.983-9560G>T
ENST00000642455.1:c.1055G>T	ENSP00000493827.1:p.Gly352Val
ENST00000642751.1:c.928G>T
ENST00000642999.1:c.896G>T	ENSP00000496589.1:p.Gly299Val
ENST00000643327.1:c.313G>T
ENST00000643334.1:c.734G>T
ENST00000644408.1:c.1030G>T
ENST00000644954.1:c.800G>T	ENSP00000494312.1:p.Gly267Val
ENST00000645159.1:n.506G>T
ENST00000645550.1:n.367G>T
ENST00000645671.1:c.604G>T
ENST00000645730.1:c.501G>T
ENST00000646082.1:c.800G>T
ENST00000646571.1:c.1058G>T	ENSP00000495015.1:p.Gly353Val
ENST00000647007.1:n.846G>T
ENST00000647133.1:c.674-1405G>T
ENST00000315285.7:c.1154G>T	ENSP00000320885.3:p.Gly385Val
ENST00000345662.5:c.1058G>T	ENSP00000340817.1:p.Gly353Val
ENST00000615843.4:c.1154G>T	ENSP00000480893.1:p.Gly385Val
ENST00000621856.1:c.896G>T	ENSP00000482496.1:p.Gly299Val
NM_014946.3:c.1154G>T , LRG_714t1:c.1154G>T	NP_055761.2:p.Gly385Val
NM_199436.1:c.1058G>T	NP_955468.1:p.Gly353Val
XM_005264516.3:c.1151G>T	XP_005264573.1:p.Gly384Val
XM_011533067.1:c.1154G>T	XP_011531369.1:p.Gly385Val
NM_001363823.1:c.1151G>T	NP_001350752.1:p.Gly384Val
NM_001363875.1:c.1055G>T	NP_001350804.1:p.Gly352Val
XM_005264516.5:c.1151G>T	XP_005264573.1:p.Gly384Val
XM_011533067.2:c.1154G>T	XP_011531369.1:p.Gly385Val
XM_017004778.2:c.1058G>T	XP_016860267.1:p.Gly353Val
NM_001363823.2:c.1151G>T	NP_001350752.1:p.Gly384Val
NM_001363875.2:c.1055G>T	NP_001350804.1:p.Gly352Val
NM_001377959.1:c.1058G>T	NP_001364888.1:p.Gly353Val
NM_014946.4:c.1154G>T MANE Select	NP_055761.2:p.Gly385Val
NM_199436.2:c.1058G>T	NP_955468.1:p.Gly353Val