Canonical Allele Identifier: CA2523039916

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32146590_32146591insAT , CM000664.2:g.32146590_32146591insAT	GRCh38
NC_000002.11:g.32371659_32371660insAT , CM000664.1:g.32371659_32371660insAT	GRCh37
NC_000002.10:g.32225163_32225164insAT	NCBI36
NG_008730.1:g.87980_87981insAT , LRG_714:g.87980_87981insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*1348-628_*1348-627insAT	ENSP00000515816.1:n.*1348-628_*1348-627insAT
ENST00000315285.9:c.1688-628_1688-627insAT MANE Select	ENSP00000320885.3:n.1688-628_1688-627insAT
ENST00000621856.2:c.1685-628_1685-627insAT	ENSP00000482496.2:n.1685-628_1685-627insAT
ENST00000642281.1:c.1425-628_1425-627insAT
ENST00000642455.1:c.1589-628_1589-627insAT	ENSP00000493827.1:n.1589-628_1589-627insAT
ENST00000642751.1:c.1391-628_1391-627insAT
ENST00000642999.1:c.1430-628_1430-627insAT	ENSP00000496589.1:n.1430-628_1430-627insAT
ENST00000643334.1:c.1268-628_1268-627insAT
ENST00000644408.1:c.1564-605_1564-604insAT
ENST00000644954.1:c.1334-628_1334-627insAT	ENSP00000494312.1:n.1334-628_1334-627insAT
ENST00000645159.1:n.2425-628_2425-627insAT
ENST00000645671.1:c.1067-628_1067-627insAT
ENST00000645730.1:c.867-628_867-627insAT
ENST00000646082.1:c.1334-628_1334-627insAT
ENST00000646571.1:c.1592-628_1592-627insAT	ENSP00000495015.1:n.1592-628_1592-627insAT
ENST00000647007.1:n.1380-628_1380-627insAT
ENST00000647133.1:c.1188-628_1188-627insAT
ENST00000315285.7:c.1688-628_1688-627insAT	ENSP00000320885.3:n.1688-628_1688-627insAT
ENST00000345662.5:c.1592-628_1592-627insAT	ENSP00000340817.1:n.1592-628_1592-627insAT
ENST00000615843.4:c.1688-628_1688-627insAT	ENSP00000480893.1:n.1688-628_1688-627insAT
ENST00000621856.1:c.1430-628_1430-627insAT	ENSP00000482496.1:n.1430-628_1430-627insAT
NM_014946.3:c.1688-628_1688-627insAT , LRG_714t1:c.1688-628_1688-627insAT	NP_055761.2:n.1688-628_1688-627insAT
NM_199436.1:c.1592-628_1592-627insAT	NP_955468.1:n.1592-628_1592-627insAT
XM_005264516.3:c.1685-628_1685-627insAT	XP_005264573.1:n.1685-628_1685-627insAT
XM_011533067.1:c.1617-628_1617-627insAT	XP_011531369.1:n.1617-628_1617-627insAT
NM_001363823.1:c.1685-628_1685-627insAT	NP_001350752.1:n.1685-628_1685-627insAT
NM_001363875.1:c.1589-628_1589-627insAT	NP_001350804.1:n.1589-628_1589-627insAT
XM_005264516.5:c.1685-628_1685-627insAT	XP_005264573.1:n.1685-628_1685-627insAT
XM_011533067.2:c.1617-628_1617-627insAT	XP_011531369.1:n.1617-628_1617-627insAT
XM_017004778.2:c.1521-628_1521-627insAT	XP_016860267.1:n.1521-628_1521-627insAT
NM_001363823.2:c.1685-628_1685-627insAT	NP_001350752.1:n.1685-628_1685-627insAT
NM_001363875.2:c.1589-628_1589-627insAT	NP_001350804.1:n.1589-628_1589-627insAT
NM_001377959.1:c.1521-628_1521-627insAT	NP_001364888.1:n.1521-628_1521-627insAT
NM_014946.4:c.1688-628_1688-627insAT MANE Select	NP_055761.2:n.1688-628_1688-627insAT
NM_199436.2:c.1592-628_1592-627insAT	NP_955468.1:n.1592-628_1592-627insAT