Canonical Allele Identifier: CA346501352

Gene: SPAST

Linked Data

• MyVariant Identifiers: chr2:g.32352093T>G (hg19) ; chr2:g.32127024T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32127024T>G , CM000664.2:g.32127024T>G	GRCh38
NC_000002.11:g.32352093T>G , CM000664.1:g.32352093T>G	GRCh37
NC_000002.10:g.32205597T>G	NCBI36
NG_008730.1:g.68414T>G , LRG_714:g.68414T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*833+2T>G	ENSP00000515816.1:n.*833+2T>G
ENST00000315285.9:c.1173+2T>G MANE Select	ENSP00000320885.3:n.1173+2T>G
ENST00000621856.2:c.1170+2T>G	ENSP00000482496.2:n.1170+2T>G
ENST00000642281.1:c.983-9539T>G
ENST00000642455.1:c.1074+2T>G	ENSP00000493827.1:n.1074+2T>G
ENST00000642751.1:c.947+2T>G
ENST00000642999.1:c.915+2T>G	ENSP00000496589.1:n.915+2T>G
ENST00000643327.1:c.332+2T>G
ENST00000643334.1:c.753+2T>G
ENST00000644408.1:c.1049+2T>G
ENST00000644954.1:c.819+2T>G	ENSP00000494312.1:n.819+2T>G
ENST00000645159.1:n.527T>G
ENST00000645550.1:n.386+2T>G
ENST00000645671.1:c.623+2T>G
ENST00000645730.1:c.520+2T>G
ENST00000646082.1:c.819+2T>G
ENST00000646571.1:c.1077+2T>G	ENSP00000495015.1:n.1077+2T>G
ENST00000647007.1:n.865+2T>G
ENST00000647133.1:c.674-1384T>G
ENST00000315285.7:c.1173+2T>G	ENSP00000320885.3:n.1173+2T>G
ENST00000345662.5:c.1077+2T>G	ENSP00000340817.1:n.1077+2T>G
ENST00000615843.4:c.1173+2T>G	ENSP00000480893.1:n.1173+2T>G
ENST00000621856.1:c.915+2T>G	ENSP00000482496.1:n.915+2T>G
NM_014946.3:c.1173+2T>G , LRG_714t1:c.1173+2T>G	NP_055761.2:n.1173+2T>G
NM_199436.1:c.1077+2T>G	NP_955468.1:n.1077+2T>G
XM_005264516.3:c.1170+2T>G	XP_005264573.1:n.1170+2T>G
XM_011533067.1:c.1173+2T>G	XP_011531369.1:n.1173+2T>G
NM_001363823.1:c.1170+2T>G	NP_001350752.1:n.1170+2T>G
NM_001363875.1:c.1074+2T>G	NP_001350804.1:n.1074+2T>G
XM_005264516.5:c.1170+2T>G	XP_005264573.1:n.1170+2T>G
XM_011533067.2:c.1173+2T>G	XP_011531369.1:n.1173+2T>G
XM_017004778.2:c.1077+2T>G	XP_016860267.1:n.1077+2T>G
NM_001363823.2:c.1170+2T>G	NP_001350752.1:n.1170+2T>G
NM_001363875.2:c.1074+2T>G	NP_001350804.1:n.1074+2T>G
NM_001377959.1:c.1077+2T>G	NP_001364888.1:n.1077+2T>G
NM_014946.4:c.1173+2T>G MANE Select	NP_055761.2:n.1173+2T>G
NM_199436.2:c.1077+2T>G	NP_955468.1:n.1077+2T>G