Canonical Allele Identifier: CA2658523351
Gene: SPAST HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32147122_32147123insC , CM000664.2:g.32147122_32147123insC GRCh38
NC_000002.11:g.32372191_32372192insC , CM000664.1:g.32372191_32372192insC GRCh37
NC_000002.10:g.32225695_32225696insC NCBI36
NG_008730.1:g.88512_88513insC , LRG_714:g.88512_88513insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.*1348-96_*1348-95insC ENSP00000515816.1:n.*1348-96_*1348-95insC
ENST00000315285.9:c.1688-96_1688-95insC MANE Select ENSP00000320885.3:n.1688-96_1688-95insC
ENST00000621856.2:c.1685-96_1685-95insC ENSP00000482496.2:n.1685-96_1685-95insC
ENST00000642281.1:c.1425-96_1425-95insC
ENST00000642455.1:c.1589-96_1589-95insC ENSP00000493827.1:n.1589-96_1589-95insC
ENST00000642751.1:c.1391-96_1391-95insC
ENST00000642999.1:c.1430-96_1430-95insC ENSP00000496589.1:n.1430-96_1430-95insC
ENST00000643334.1:c.1268-96_1268-95insC
ENST00000644408.1:c.1564-73_1564-72insC
ENST00000644954.1:c.1334-96_1334-95insC ENSP00000494312.1:n.1334-96_1334-95insC
ENST00000645159.1:n.2425-96_2425-95insC
ENST00000645671.1:c.1067-96_1067-95insC
ENST00000645730.1:c.867-96_867-95insC
ENST00000646082.1:c.1334-96_1334-95insC
ENST00000646571.1:c.1592-96_1592-95insC ENSP00000495015.1:n.1592-96_1592-95insC
ENST00000647007.1:n.1380-96_1380-95insC
ENST00000647133.1:c.1188-96_1188-95insC
ENST00000315285.7:c.1688-96_1688-95insC ENSP00000320885.3:n.1688-96_1688-95insC
ENST00000345662.5:c.1592-96_1592-95insC ENSP00000340817.1:n.1592-96_1592-95insC
ENST00000615843.4:c.1688-96_1688-95insC ENSP00000480893.1:n.1688-96_1688-95insC
ENST00000621856.1:c.1430-96_1430-95insC ENSP00000482496.1:n.1430-96_1430-95insC
NM_014946.3:c.1688-96_1688-95insC , LRG_714t1:c.1688-96_1688-95insC NP_055761.2:n.1688-96_1688-95insC
NM_199436.1:c.1592-96_1592-95insC NP_955468.1:n.1592-96_1592-95insC
XM_005264516.3:c.1685-96_1685-95insC XP_005264573.1:n.1685-96_1685-95insC
XM_011533067.1:c.1617-96_1617-95insC XP_011531369.1:n.1617-96_1617-95insC
NM_001363823.1:c.1685-96_1685-95insC NP_001350752.1:n.1685-96_1685-95insC
NM_001363875.1:c.1589-96_1589-95insC NP_001350804.1:n.1589-96_1589-95insC
XM_005264516.5:c.1685-96_1685-95insC XP_005264573.1:n.1685-96_1685-95insC
XM_011533067.2:c.1617-96_1617-95insC XP_011531369.1:n.1617-96_1617-95insC
XM_017004778.2:c.1521-96_1521-95insC XP_016860267.1:n.1521-96_1521-95insC
NM_001363823.2:c.1685-96_1685-95insC NP_001350752.1:n.1685-96_1685-95insC
NM_001363875.2:c.1589-96_1589-95insC NP_001350804.1:n.1589-96_1589-95insC
NM_001377959.1:c.1521-96_1521-95insC NP_001364888.1:n.1521-96_1521-95insC
NM_014946.4:c.1688-96_1688-95insC MANE Select NP_055761.2:n.1688-96_1688-95insC
NM_199436.2:c.1592-96_1592-95insC NP_955468.1:n.1592-96_1592-95insC