Canonical Allele Identifier: CA2749394956

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32146850_32146851insAA , CM000664.2:g.32146850_32146851insAA	GRCh38
NC_000002.11:g.32371919_32371920insAA , CM000664.1:g.32371919_32371920insAA	GRCh37
NC_000002.10:g.32225423_32225424insAA	NCBI36
NG_008730.1:g.88240_88241insAA , LRG_714:g.88240_88241insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*1348-368_*1348-367insAA	ENSP00000515816.1:n.*1348-368_*1348-367insAA
ENST00000315285.9:c.1688-368_1688-367insAA MANE Select	ENSP00000320885.3:n.1688-368_1688-367insAA
ENST00000621856.2:c.1685-368_1685-367insAA	ENSP00000482496.2:n.1685-368_1685-367insAA
ENST00000642281.1:c.1425-368_1425-367insAA
ENST00000642455.1:c.1589-368_1589-367insAA	ENSP00000493827.1:n.1589-368_1589-367insAA
ENST00000642751.1:c.1391-368_1391-367insAA
ENST00000642999.1:c.1430-368_1430-367insAA	ENSP00000496589.1:n.1430-368_1430-367insAA
ENST00000643334.1:c.1268-368_1268-367insAA
ENST00000644408.1:c.1564-345_1564-344insAA
ENST00000644954.1:c.1334-368_1334-367insAA	ENSP00000494312.1:n.1334-368_1334-367insAA
ENST00000645159.1:n.2425-368_2425-367insAA
ENST00000645671.1:c.1067-368_1067-367insAA
ENST00000645730.1:c.867-368_867-367insAA
ENST00000646082.1:c.1334-368_1334-367insAA
ENST00000646571.1:c.1592-368_1592-367insAA	ENSP00000495015.1:n.1592-368_1592-367insAA
ENST00000647007.1:n.1380-368_1380-367insAA
ENST00000647133.1:c.1188-368_1188-367insAA
ENST00000315285.7:c.1688-368_1688-367insAA	ENSP00000320885.3:n.1688-368_1688-367insAA
ENST00000345662.5:c.1592-368_1592-367insAA	ENSP00000340817.1:n.1592-368_1592-367insAA
ENST00000615843.4:c.1688-368_1688-367insAA	ENSP00000480893.1:n.1688-368_1688-367insAA
ENST00000621856.1:c.1430-368_1430-367insAA	ENSP00000482496.1:n.1430-368_1430-367insAA
NM_014946.3:c.1688-368_1688-367insAA , LRG_714t1:c.1688-368_1688-367insAA	NP_055761.2:n.1688-368_1688-367insAA
NM_199436.1:c.1592-368_1592-367insAA	NP_955468.1:n.1592-368_1592-367insAA
XM_005264516.3:c.1685-368_1685-367insAA	XP_005264573.1:n.1685-368_1685-367insAA
XM_011533067.1:c.1617-368_1617-367insAA	XP_011531369.1:n.1617-368_1617-367insAA
NM_001363823.1:c.1685-368_1685-367insAA	NP_001350752.1:n.1685-368_1685-367insAA
NM_001363875.1:c.1589-368_1589-367insAA	NP_001350804.1:n.1589-368_1589-367insAA
XM_005264516.5:c.1685-368_1685-367insAA	XP_005264573.1:n.1685-368_1685-367insAA
XM_011533067.2:c.1617-368_1617-367insAA	XP_011531369.1:n.1617-368_1617-367insAA
XM_017004778.2:c.1521-368_1521-367insAA	XP_016860267.1:n.1521-368_1521-367insAA
NM_001363823.2:c.1685-368_1685-367insAA	NP_001350752.1:n.1685-368_1685-367insAA
NM_001363875.2:c.1589-368_1589-367insAA	NP_001350804.1:n.1589-368_1589-367insAA
NM_001377959.1:c.1521-368_1521-367insAA	NP_001364888.1:n.1521-368_1521-367insAA
NM_014946.4:c.1688-368_1688-367insAA MANE Select	NP_055761.2:n.1688-368_1688-367insAA
NM_199436.2:c.1592-368_1592-367insAA	NP_955468.1:n.1592-368_1592-367insAA