Canonical Allele Identifier: CA767786513

Gene: SPAST

Linked Data

• dbSNP Id: rs1169269522
• gnomAD v3: 2-32126736-C-G
• gnomAD v4: 2-32126736-C-G
• MyVariant Identifiers: chr2:g.32351805C>G (hg19) ; chr2:g.32126736C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32126736C>G , CM000664.2:g.32126736C>G	GRCh38
NC_000002.11:g.32351805C>G , CM000664.1:g.32351805C>G	GRCh37
NC_000002.10:g.32205309C>G	NCBI36
NG_008730.1:g.68126C>G , LRG_714:g.68126C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*759-212C>G	ENSP00000515816.1:n.*759-212C>G
ENST00000315285.9:c.1099-212C>G MANE Select	ENSP00000320885.3:n.1099-212C>G
ENST00000621856.2:c.1096-212C>G	ENSP00000482496.2:n.1096-212C>G
ENST00000642281.1:c.983-9827C>G
ENST00000642455.1:c.1000-212C>G	ENSP00000493827.1:n.1000-212C>G
ENST00000642751.1:c.873-212C>G
ENST00000642999.1:c.841-212C>G	ENSP00000496589.1:n.841-212C>G
ENST00000643327.1:c.258-212C>G
ENST00000643334.1:c.679-212C>G
ENST00000644408.1:c.975-212C>G
ENST00000644954.1:c.745-212C>G	ENSP00000494312.1:n.745-212C>G
ENST00000645159.1:n.239C>G
ENST00000645550.1:n.100C>G
ENST00000645671.1:c.549-212C>G
ENST00000645730.1:c.446-212C>G
ENST00000646082.1:c.745-212C>G
ENST00000646571.1:c.1003-212C>G	ENSP00000495015.1:n.1003-212C>G
ENST00000647007.1:n.791-212C>G
ENST00000647133.1:c.674-1672C>G
ENST00000315285.7:c.1099-212C>G	ENSP00000320885.3:n.1099-212C>G
ENST00000345662.5:c.1003-212C>G	ENSP00000340817.1:n.1003-212C>G
ENST00000615843.4:c.1099-212C>G	ENSP00000480893.1:n.1099-212C>G
ENST00000621856.1:c.841-212C>G	ENSP00000482496.1:n.841-212C>G
NM_014946.3:c.1099-212C>G , LRG_714t1:c.1099-212C>G	NP_055761.2:n.1099-212C>G
NM_199436.1:c.1003-212C>G	NP_955468.1:n.1003-212C>G
XM_005264516.3:c.1096-212C>G	XP_005264573.1:n.1096-212C>G
XM_011533067.1:c.1099-212C>G	XP_011531369.1:n.1099-212C>G
NM_001363823.1:c.1096-212C>G	NP_001350752.1:n.1096-212C>G
NM_001363875.1:c.1000-212C>G	NP_001350804.1:n.1000-212C>G
XM_005264516.5:c.1096-212C>G	XP_005264573.1:n.1096-212C>G
XM_011533067.2:c.1099-212C>G	XP_011531369.1:n.1099-212C>G
XM_017004778.2:c.1003-212C>G	XP_016860267.1:n.1003-212C>G
NM_001363823.2:c.1096-212C>G	NP_001350752.1:n.1096-212C>G
NM_001363875.2:c.1000-212C>G	NP_001350804.1:n.1000-212C>G
NM_001377959.1:c.1003-212C>G	NP_001364888.1:n.1003-212C>G
NM_014946.4:c.1099-212C>G MANE Select	NP_055761.2:n.1099-212C>G
NM_199436.2:c.1003-212C>G	NP_955468.1:n.1003-212C>G