Canonical Allele Identifier: CA1242506813
Gene: SPAST HGNC NCBI

Linked Data

dbSNP Id: rs1679904573

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32146877_32146878insT , CM000664.2:g.32146877_32146878insT GRCh38
NC_000002.11:g.32371946_32371947insT , CM000664.1:g.32371946_32371947insT GRCh37
NC_000002.10:g.32225450_32225451insT NCBI36
NG_008730.1:g.88267_88268insT , LRG_714:g.88267_88268insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.*1348-341_*1348-340insT ENSP00000515816.1:n.*1348-341_*1348-340insT
ENST00000315285.9:c.1688-341_1688-340insT MANE Select ENSP00000320885.3:n.1688-341_1688-340insT
ENST00000621856.2:c.1685-341_1685-340insT ENSP00000482496.2:n.1685-341_1685-340insT
ENST00000642281.1:c.1425-341_1425-340insT
ENST00000642455.1:c.1589-341_1589-340insT ENSP00000493827.1:n.1589-341_1589-340insT
ENST00000642751.1:c.1391-341_1391-340insT
ENST00000642999.1:c.1430-341_1430-340insT ENSP00000496589.1:n.1430-341_1430-340insT
ENST00000643334.1:c.1268-341_1268-340insT
ENST00000644408.1:c.1564-318_1564-317insT
ENST00000644954.1:c.1334-341_1334-340insT ENSP00000494312.1:n.1334-341_1334-340insT
ENST00000645159.1:n.2425-341_2425-340insT
ENST00000645671.1:c.1067-341_1067-340insT
ENST00000645730.1:c.867-341_867-340insT
ENST00000646082.1:c.1334-341_1334-340insT
ENST00000646571.1:c.1592-341_1592-340insT ENSP00000495015.1:n.1592-341_1592-340insT
ENST00000647007.1:n.1380-341_1380-340insT
ENST00000647133.1:c.1188-341_1188-340insT
ENST00000315285.7:c.1688-341_1688-340insT ENSP00000320885.3:n.1688-341_1688-340insT
ENST00000345662.5:c.1592-341_1592-340insT ENSP00000340817.1:n.1592-341_1592-340insT
ENST00000615843.4:c.1688-341_1688-340insT ENSP00000480893.1:n.1688-341_1688-340insT
ENST00000621856.1:c.1430-341_1430-340insT ENSP00000482496.1:n.1430-341_1430-340insT
NM_014946.3:c.1688-341_1688-340insT , LRG_714t1:c.1688-341_1688-340insT NP_055761.2:n.1688-341_1688-340insT
NM_199436.1:c.1592-341_1592-340insT NP_955468.1:n.1592-341_1592-340insT
XM_005264516.3:c.1685-341_1685-340insT XP_005264573.1:n.1685-341_1685-340insT
XM_011533067.1:c.1617-341_1617-340insT XP_011531369.1:n.1617-341_1617-340insT
NM_001363823.1:c.1685-341_1685-340insT NP_001350752.1:n.1685-341_1685-340insT
NM_001363875.1:c.1589-341_1589-340insT NP_001350804.1:n.1589-341_1589-340insT
XM_005264516.5:c.1685-341_1685-340insT XP_005264573.1:n.1685-341_1685-340insT
XM_011533067.2:c.1617-341_1617-340insT XP_011531369.1:n.1617-341_1617-340insT
XM_017004778.2:c.1521-341_1521-340insT XP_016860267.1:n.1521-341_1521-340insT
NM_001363823.2:c.1685-341_1685-340insT NP_001350752.1:n.1685-341_1685-340insT
NM_001363875.2:c.1589-341_1589-340insT NP_001350804.1:n.1589-341_1589-340insT
NM_001377959.1:c.1521-341_1521-340insT NP_001364888.1:n.1521-341_1521-340insT
NM_014946.4:c.1688-341_1688-340insT MANE Select NP_055761.2:n.1688-341_1688-340insT
NM_199436.2:c.1592-341_1592-340insT NP_955468.1:n.1592-341_1592-340insT