Canonical Allele Identifier: CA2840092999

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32136723T>A , CM000664.2:g.32136723T>A	GRCh38
NC_000002.11:g.32361792T>A , CM000664.1:g.32361792T>A	GRCh37
NC_000002.10:g.32215296T>A	NCBI36
NG_008730.1:g.78113T>A , LRG_714:g.78113T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*981+85T>A	ENSP00000515816.1:n.*981+85T>A
ENST00000315285.9:c.1321+85T>A MANE Select	ENSP00000320885.3:n.1321+85T>A
ENST00000621856.2:c.1318+85T>A	ENSP00000482496.2:n.1318+85T>A
ENST00000642281.1:c.1058+85T>A
ENST00000642455.1:c.1222+85T>A	ENSP00000493827.1:n.1222+85T>A
ENST00000642751.1:c.1095+85T>A
ENST00000642999.1:c.1063+85T>A	ENSP00000496589.1:n.1063+85T>A
ENST00000643327.1:c.480+85T>A
ENST00000643334.1:c.901+85T>A
ENST00000644408.1:c.1197+85T>A
ENST00000644954.1:c.967+85T>A	ENSP00000494312.1:n.967+85T>A
ENST00000645159.1:n.2058+85T>A
ENST00000645671.1:c.771+85T>A
ENST00000645730.1:c.593-386T>A
ENST00000646082.1:c.967+85T>A
ENST00000646571.1:c.1225+85T>A	ENSP00000495015.1:n.1225+85T>A
ENST00000647007.1:n.1013+85T>A
ENST00000647133.1:c.821+85T>A
ENST00000315285.7:c.1321+85T>A	ENSP00000320885.3:n.1321+85T>A
ENST00000345662.5:c.1225+85T>A	ENSP00000340817.1:n.1225+85T>A
ENST00000615843.4:c.1321+85T>A	ENSP00000480893.1:n.1321+85T>A
ENST00000621856.1:c.1063+85T>A	ENSP00000482496.1:n.1063+85T>A
NM_014946.3:c.1321+85T>A , LRG_714t1:c.1321+85T>A	NP_055761.2:n.1321+85T>A
NM_199436.1:c.1225+85T>A	NP_955468.1:n.1225+85T>A
XM_005264516.3:c.1318+85T>A	XP_005264573.1:n.1318+85T>A
XM_011533067.1:c.1321+85T>A	XP_011531369.1:n.1321+85T>A
NM_001363823.1:c.1318+85T>A	NP_001350752.1:n.1318+85T>A
NM_001363875.1:c.1222+85T>A	NP_001350804.1:n.1222+85T>A
XM_005264516.5:c.1318+85T>A	XP_005264573.1:n.1318+85T>A
XM_011533067.2:c.1321+85T>A	XP_011531369.1:n.1321+85T>A
XM_017004778.2:c.1225+85T>A	XP_016860267.1:n.1225+85T>A
NM_001363823.2:c.1318+85T>A	NP_001350752.1:n.1318+85T>A
NM_001363875.2:c.1222+85T>A	NP_001350804.1:n.1222+85T>A
NM_001377959.1:c.1225+85T>A	NP_001364888.1:n.1225+85T>A
NM_014946.4:c.1321+85T>A MANE Select	NP_055761.2:n.1321+85T>A
NM_199436.2:c.1225+85T>A	NP_955468.1:n.1225+85T>A