Canonical Allele Identifier: CA1600448

Gene: SPAST

Linked Data

• ClinVar Variation Id: 335827
• ClinVar RCV Id: RCV000276579 ; RCV001848691
• dbSNP Id: rs376165443
• ExAC: 2:32288894 G / A
• gnomAD v2: 2-32288894-G-A
• gnomAD v3: 2-32063825-G-A
• gnomAD v4: 2-32063825-G-A
• MyVariant Identifiers: chr2:g.32288894G>A (hg19) ; chr2:g.32063825G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32063825G>A , CM000664.2:g.32063825G>A	GRCh38
NC_000002.11:g.32288894G>A , CM000664.1:g.32288894G>A	GRCh37
NC_000002.10:g.32142398G>A	NCBI36
NG_008730.1:g.5215G>A , LRG_714:g.5215G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.-7G>A	ENSP00000515816.1:n.-7G>A
ENST00000315285.9:c.-7G>A MANE Select	ENSP00000320885.3:n.-7G>A
ENST00000621856.2:c.-7G>A	ENSP00000482496.2:n.-7G>A
ENST00000646571.1:c.-7G>A	ENSP00000495015.1:n.-7G>A
ENST00000315285.7:c.-7G>A	ENSP00000320885.3:n.-7G>A
ENST00000345662.5:c.-7G>A	ENSP00000340817.1:n.-7G>A
ENST00000615843.4:c.-7G>A	ENSP00000480893.1:n.-7G>A
NM_014946.3:c.-7G>A , LRG_714t1:c.-7G>A	NP_055761.2:n.-7G>A
NM_199436.1:c.-7G>A	NP_955468.1:n.-7G>A
XM_005264516.3:c.-7G>A	XP_005264573.1:n.-7G>A
XM_011533067.1:c.-7G>A	XP_011531369.1:n.-7G>A
NM_001363823.1:c.-7G>A	NP_001350752.1:n.-7G>A
NM_001363875.1:c.-7G>A	NP_001350804.1:n.-7G>A
XM_011533067.2:c.-7G>A	XP_011531369.1:n.-7G>A
XM_017004778.2:c.-7G>A	XP_016860267.1:n.-7G>A
NM_001363823.2:c.-7G>A	NP_001350752.1:n.-7G>A
NM_001363875.2:c.-7G>A	NP_001350804.1:n.-7G>A
NM_001377959.1:c.-7G>A	NP_001364888.1:n.-7G>A
NM_014946.4:c.-7G>A MANE Select	NP_055761.2:n.-7G>A
NM_199436.2:c.-7G>A	NP_955468.1:n.-7G>A