Canonical Allele Identifier: CA2658520097

Gene: SPAST

Linked Data

• gnomAD v4: 2-32064284-G-GGT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32064284_32064285insGT , CM000664.2:g.32064284_32064285insGT	GRCh38
NC_000002.11:g.32289353_32289354insGT , CM000664.1:g.32289353_32289354insGT	GRCh37
NC_000002.10:g.32142857_32142858insGT	NCBI36
NG_008730.1:g.5674_5675insGT , LRG_714:g.5674_5675insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.415+38_415+39insGT	ENSP00000515816.1:n.415+38_415+39insGT
ENST00000315285.9:c.415+38_415+39insGT MANE Select	ENSP00000320885.3:n.415+38_415+39insGT
ENST00000621856.2:c.415+38_415+39insGT	ENSP00000482496.2:n.415+38_415+39insGT
ENST00000642281.1:c.299+38_299+39insGT
ENST00000642455.1:c.415+38_415+39insGT	ENSP00000493827.1:n.415+38_415+39insGT
ENST00000642751.1:c.285+38_285+39insGT
ENST00000642999.1:c.157+38_157+39insGT	ENSP00000496589.1:n.157+38_157+39insGT
ENST00000644408.1:c.291+38_291+39insGT
ENST00000644954.1:c.157+38_157+39insGT	ENSP00000494312.1:n.157+38_157+39insGT
ENST00000645400.1:c.256+38_256+39insGT	ENSP00000496306.1:n.256+38_256+39insGT
ENST00000645671.1:c.36+38_36+39insGT
ENST00000646082.1:c.249+38_249+39insGT
ENST00000646571.1:c.415+38_415+39insGT	ENSP00000495015.1:n.415+38_415+39insGT
ENST00000315285.7:c.415+38_415+39insGT	ENSP00000320885.3:n.415+38_415+39insGT
ENST00000345662.5:c.415+38_415+39insGT	ENSP00000340817.1:n.415+38_415+39insGT
ENST00000615843.4:c.415+38_415+39insGT	ENSP00000480893.1:n.415+38_415+39insGT
ENST00000621856.1:c.157+38_157+39insGT	ENSP00000482496.1:n.157+38_157+39insGT
NM_014946.3:c.415+38_415+39insGT , LRG_714t1:c.415+38_415+39insGT	NP_055761.2:n.415+38_415+39insGT
NM_199436.1:c.415+38_415+39insGT	NP_955468.1:n.415+38_415+39insGT
XM_005264516.3:c.415+38_415+39insGT	XP_005264573.1:n.415+38_415+39insGT
XM_011533067.1:c.415+38_415+39insGT	XP_011531369.1:n.415+38_415+39insGT
NM_001363823.1:c.415+38_415+39insGT	NP_001350752.1:n.415+38_415+39insGT
NM_001363875.1:c.415+38_415+39insGT	NP_001350804.1:n.415+38_415+39insGT
XM_005264516.5:c.415+38_415+39insGT	XP_005264573.1:n.415+38_415+39insGT
XM_011533067.2:c.415+38_415+39insGT	XP_011531369.1:n.415+38_415+39insGT
XM_017004778.2:c.415+38_415+39insGT	XP_016860267.1:n.415+38_415+39insGT
NM_001363823.2:c.415+38_415+39insGT	NP_001350752.1:n.415+38_415+39insGT
NM_001363875.2:c.415+38_415+39insGT	NP_001350804.1:n.415+38_415+39insGT
NM_001377959.1:c.415+38_415+39insGT	NP_001364888.1:n.415+38_415+39insGT
NM_014946.4:c.415+38_415+39insGT MANE Select	NP_055761.2:n.415+38_415+39insGT
NM_199436.2:c.415+38_415+39insGT	NP_955468.1:n.415+38_415+39insGT