Canonical Allele Identifier: CA1139656869
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 951558
ClinVar RCV Id: RCV001223514

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32127207_32128479del , CM000664.2:g.32127207_32128479del GRCh38
NC_000002.11:g.32352276_32353548del , CM000664.1:g.32352276_32353548del GRCh37
NC_000002.10:g.32205780_32207052del NCBI36
NG_008730.1:g.68597_69869del , LRG_714:g.68597_69869del

Transcript Alleles

HGVS Amino-acid change
ENST00000704289.1:c.*833+185_*905del
ENST00000315285.9:c.1173+185_1245del
ENST00000621856.2:c.1170+185_1242del
ENST00000642281.1:c.983-9356_983-8084del
ENST00000642455.1:c.1074+185_1146del
ENST00000642751.1:c.947+185_1019del
ENST00000642999.1:c.915+185_987del
ENST00000643327.1:c.332+185_404del
ENST00000643334.1:c.753+185_825del
ENST00000644408.1:c.1049+185_1121del
ENST00000644954.1:c.819+185_891del
ENST00000645159.1:n.710_1982del
ENST00000645550.1:n.386+185_458del
ENST00000645671.1:c.623+185_695del
ENST00000645730.1:c.520+185_592del
ENST00000646082.1:c.819+185_891del
ENST00000646571.1:c.1077+185_1149del
ENST00000647007.1:n.865+185_937del
ENST00000647133.1:c.674-1201_745del
ENST00000315285.7:c.1173+185_1245del
ENST00000345662.5:c.1077+185_1149del
ENST00000615843.4:c.1173+185_1245del
ENST00000621856.1:c.915+185_987del
NM_014946.3:c.1173+185_1245del , LRG_714t1:c.1173+185_1245del
NM_199436.1:c.1077+185_1149del
XM_005264516.3:c.1170+185_1242del
XM_011533067.1:c.1173+185_1245del
NM_001363823.1:c.1170+185_1242del
NM_001363875.1:c.1074+185_1146del
XM_005264516.5:c.1170+185_1242del
XM_011533067.2:c.1173+185_1245del
XM_017004778.2:c.1077+185_1149del
NM_001363823.2:c.1170+185_1242del
NM_001363875.2:c.1074+185_1146del
NM_001377959.1:c.1077+185_1149del
NM_014946.4:c.1173+185_1245del
NM_199436.2:c.1077+185_1149del