Canonical Allele Identifier: CA2658520100

Gene: SPAST

Linked Data

• gnomAD v4: 2-32064285-A-ATT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32064285_32064286insTT , CM000664.2:g.32064285_32064286insTT	GRCh38
NC_000002.11:g.32289354_32289355insTT , CM000664.1:g.32289354_32289355insTT	GRCh37
NC_000002.10:g.32142858_32142859insTT	NCBI36
NG_008730.1:g.5675_5676insTT , LRG_714:g.5675_5676insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.415+39_415+40insTT	ENSP00000515816.1:n.415+39_415+40insTT
ENST00000315285.9:c.415+39_415+40insTT MANE Select	ENSP00000320885.3:n.415+39_415+40insTT
ENST00000621856.2:c.415+39_415+40insTT	ENSP00000482496.2:n.415+39_415+40insTT
ENST00000642281.1:c.299+39_299+40insTT
ENST00000642455.1:c.415+39_415+40insTT	ENSP00000493827.1:n.415+39_415+40insTT
ENST00000642751.1:c.285+39_285+40insTT
ENST00000642999.1:c.157+39_157+40insTT	ENSP00000496589.1:n.157+39_157+40insTT
ENST00000644408.1:c.291+39_291+40insTT
ENST00000644954.1:c.157+39_157+40insTT	ENSP00000494312.1:n.157+39_157+40insTT
ENST00000645400.1:c.256+39_256+40insTT	ENSP00000496306.1:n.256+39_256+40insTT
ENST00000645671.1:c.36+39_36+40insTT
ENST00000646082.1:c.249+39_249+40insTT
ENST00000646571.1:c.415+39_415+40insTT	ENSP00000495015.1:n.415+39_415+40insTT
ENST00000315285.7:c.415+39_415+40insTT	ENSP00000320885.3:n.415+39_415+40insTT
ENST00000345662.5:c.415+39_415+40insTT	ENSP00000340817.1:n.415+39_415+40insTT
ENST00000615843.4:c.415+39_415+40insTT	ENSP00000480893.1:n.415+39_415+40insTT
ENST00000621856.1:c.157+39_157+40insTT	ENSP00000482496.1:n.157+39_157+40insTT
NM_014946.3:c.415+39_415+40insTT , LRG_714t1:c.415+39_415+40insTT	NP_055761.2:n.415+39_415+40insTT
NM_199436.1:c.415+39_415+40insTT	NP_955468.1:n.415+39_415+40insTT
XM_005264516.3:c.415+39_415+40insTT	XP_005264573.1:n.415+39_415+40insTT
XM_011533067.1:c.415+39_415+40insTT	XP_011531369.1:n.415+39_415+40insTT
NM_001363823.1:c.415+39_415+40insTT	NP_001350752.1:n.415+39_415+40insTT
NM_001363875.1:c.415+39_415+40insTT	NP_001350804.1:n.415+39_415+40insTT
XM_005264516.5:c.415+39_415+40insTT	XP_005264573.1:n.415+39_415+40insTT
XM_011533067.2:c.415+39_415+40insTT	XP_011531369.1:n.415+39_415+40insTT
XM_017004778.2:c.415+39_415+40insTT	XP_016860267.1:n.415+39_415+40insTT
NM_001363823.2:c.415+39_415+40insTT	NP_001350752.1:n.415+39_415+40insTT
NM_001363875.2:c.415+39_415+40insTT	NP_001350804.1:n.415+39_415+40insTT
NM_001377959.1:c.415+39_415+40insTT	NP_001364888.1:n.415+39_415+40insTT
NM_014946.4:c.415+39_415+40insTT MANE Select	NP_055761.2:n.415+39_415+40insTT
NM_199436.2:c.415+39_415+40insTT	NP_955468.1:n.415+39_415+40insTT