Canonical Allele Identifier: CA346502477

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32137155A>G , CM000664.2:g.32137155A>G	GRCh38
NC_000002.11:g.32362224A>G , CM000664.1:g.32362224A>G	GRCh37
NC_000002.10:g.32215728A>G	NCBI36
NG_008730.1:g.78545A>G , LRG_714:g.78545A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_014946.4:c.1460A>G MANE Select	NP_055761.2:p.Asn487Ser
ENST00000315285.9:c.1460A>G MANE Select	ENSP00000320885.3:p.Asn487Ser
NM_001363823.1:c.1457A>G	NP_001350752.1:p.Asn486Ser
NM_001363823.2:c.1457A>G	NP_001350752.1:p.Asn486Ser
NM_001363875.1:c.1361A>G	NP_001350804.1:p.Asn454Ser
NM_001363875.2:c.1361A>G	NP_001350804.1:p.Asn454Ser
NM_001377959.1:c.1364A>G	NP_001364888.1:p.Asn455Ser
NM_014946.3:c.1460A>G , LRG_714t1:c.1460A>G	NP_055761.2:p.Asn487Ser
NM_199436.1:c.1364A>G	NP_955468.1:p.Asn455Ser
NM_199436.2:c.1364A>G	NP_955468.1:p.Asn455Ser
ENST00000315285.7:c.1460A>G	ENSP00000320885.3:p.Asn487Ser
ENST00000345662.5:c.1364A>G	ENSP00000340817.1:p.Asn455Ser
ENST00000615843.4:c.1460A>G	ENSP00000480893.1:p.Asn487Ser
ENST00000621856.1:c.1202A>G	ENSP00000482496.1:p.Asn401Ser
ENST00000621856.2:c.1457A>G	ENSP00000482496.2:p.Asn486Ser
ENST00000642281.1:c.1197A>G
ENST00000642455.1:c.1361A>G	ENSP00000493827.1:p.Asn454Ser
ENST00000642751.1:c.1234A>G
ENST00000642999.1:c.1202A>G	ENSP00000496589.1:p.Asn401Ser
ENST00000643327.1:c.527A>G
ENST00000643334.1:c.1040A>G
ENST00000644408.1:c.1336A>G
ENST00000644954.1:c.1106A>G	ENSP00000494312.1:p.Asn369Ser
ENST00000645159.1:n.2197A>G
ENST00000645671.1:c.910A>G
ENST00000645730.1:c.639A>G
ENST00000646082.1:c.1106A>G
ENST00000646571.1:c.1364A>G	ENSP00000495015.1:p.Asn455Ser
ENST00000647007.1:n.1152A>G
ENST00000647133.1:c.960A>G
ENST00000704289.1:c.*1120A>G	ENSP00000515816.1:n.*1120A>G
XM_005264516.3:c.1457A>G	XP_005264573.1:p.Asn486Ser
XM_005264516.5:c.1457A>G	XP_005264573.1:p.Asn486Ser
XM_011533067.1:c.1460A>G	XP_011531369.1:p.Asn487Ser
XM_011533067.2:c.1460A>G	XP_011531369.1:p.Asn487Ser
XM_017004778.2:c.1364A>G	XP_016860267.1:p.Asn455Ser