Canonical Allele Identifier: CA2831204762

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32146881_32146882insCAACCCCC , CM000664.2:g.32146881_32146882insCAACCCCC	GRCh38
NC_000002.11:g.32371950_32371951insCAACCCCC , CM000664.1:g.32371950_32371951insCAACCCCC	GRCh37
NC_000002.10:g.32225454_32225455insCAACCCCC	NCBI36
NG_008730.1:g.88271_88272insCAACCCCC , LRG_714:g.88271_88272insCAACCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*1348-337_*1348-336insCAACCCCC	ENSP00000515816.1:n.*1348-337_*1348-336insCAACCCCC
ENST00000315285.9:c.1688-337_1688-336insCAACCCCC MANE Select	ENSP00000320885.3:n.1688-337_1688-336insCAACCCCC
ENST00000621856.2:c.1685-337_1685-336insCAACCCCC	ENSP00000482496.2:n.1685-337_1685-336insCAACCCCC
ENST00000642281.1:c.1425-337_1425-336insCAACCCCC
ENST00000642455.1:c.1589-337_1589-336insCAACCCCC	ENSP00000493827.1:n.1589-337_1589-336insCAACCCCC
ENST00000642751.1:c.1391-337_1391-336insCAACCCCC
ENST00000642999.1:c.1430-337_1430-336insCAACCCCC	ENSP00000496589.1:n.1430-337_1430-336insCAACCCCC
ENST00000643334.1:c.1268-337_1268-336insCAACCCCC
ENST00000644408.1:c.1564-314_1564-313insCAACCCCC
ENST00000644954.1:c.1334-337_1334-336insCAACCCCC	ENSP00000494312.1:n.1334-337_1334-336insCAACCCCC
ENST00000645159.1:n.2425-337_2425-336insCAACCCCC
ENST00000645671.1:c.1067-337_1067-336insCAACCCCC
ENST00000645730.1:c.867-337_867-336insCAACCCCC
ENST00000646082.1:c.1334-337_1334-336insCAACCCCC
ENST00000646571.1:c.1592-337_1592-336insCAACCCCC	ENSP00000495015.1:n.1592-337_1592-336insCAACCCCC
ENST00000647007.1:n.1380-337_1380-336insCAACCCCC
ENST00000647133.1:c.1188-337_1188-336insCAACCCCC
ENST00000315285.7:c.1688-337_1688-336insCAACCCCC	ENSP00000320885.3:n.1688-337_1688-336insCAACCCCC
ENST00000345662.5:c.1592-337_1592-336insCAACCCCC	ENSP00000340817.1:n.1592-337_1592-336insCAACCCCC
ENST00000615843.4:c.1688-337_1688-336insCAACCCCC	ENSP00000480893.1:n.1688-337_1688-336insCAACCCCC
ENST00000621856.1:c.1430-337_1430-336insCAACCCCC	ENSP00000482496.1:n.1430-337_1430-336insCAACCCCC
NM_014946.3:c.1688-337_1688-336insCAACCCCC , LRG_714t1:c.1688-337_1688-336insCAACCCCC	NP_055761.2:n.1688-337_1688-336insCAACCCCC
NM_199436.1:c.1592-337_1592-336insCAACCCCC	NP_955468.1:n.1592-337_1592-336insCAACCCCC
XM_005264516.3:c.1685-337_1685-336insCAACCCCC	XP_005264573.1:n.1685-337_1685-336insCAACCCCC
XM_011533067.1:c.1617-337_1617-336insCAACCCCC	XP_011531369.1:n.1617-337_1617-336insCAACCCCC
NM_001363823.1:c.1685-337_1685-336insCAACCCCC	NP_001350752.1:n.1685-337_1685-336insCAACCCCC
NM_001363875.1:c.1589-337_1589-336insCAACCCCC	NP_001350804.1:n.1589-337_1589-336insCAACCCCC
XM_005264516.5:c.1685-337_1685-336insCAACCCCC	XP_005264573.1:n.1685-337_1685-336insCAACCCCC
XM_011533067.2:c.1617-337_1617-336insCAACCCCC	XP_011531369.1:n.1617-337_1617-336insCAACCCCC
XM_017004778.2:c.1521-337_1521-336insCAACCCCC	XP_016860267.1:n.1521-337_1521-336insCAACCCCC
NM_001363823.2:c.1685-337_1685-336insCAACCCCC	NP_001350752.1:n.1685-337_1685-336insCAACCCCC
NM_001363875.2:c.1589-337_1589-336insCAACCCCC	NP_001350804.1:n.1589-337_1589-336insCAACCCCC
NM_001377959.1:c.1521-337_1521-336insCAACCCCC	NP_001364888.1:n.1521-337_1521-336insCAACCCCC
NM_014946.4:c.1688-337_1688-336insCAACCCCC MANE Select	NP_055761.2:n.1688-337_1688-336insCAACCCCC
NM_199436.2:c.1592-337_1592-336insCAACCCCC	NP_955468.1:n.1592-337_1592-336insCAACCCCC