Canonical Allele Identifier: CA2586964706
Gene: SPAST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32128408_32128414del , CM000664.2:g.32128408_32128414del GRCh38
NC_000002.11:g.32353477_32353483del , CM000664.1:g.32353477_32353483del GRCh37
NC_000002.10:g.32206981_32206987del NCBI36
NG_008730.1:g.69798_69804del , LRG_714:g.69798_69804del

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.*834_*840del
ENST00000315285.9:c.1174_1180del
ENST00000621856.2:c.1171_1177del
ENST00000642281.1:c.983-8155_983-8149del
ENST00000642455.1:c.1075_1081del
ENST00000642751.1:c.948_954del
ENST00000642999.1:c.916_922del
ENST00000643327.1:c.333_339del
ENST00000643334.1:c.754_760del
ENST00000644408.1:c.1050_1056del
ENST00000644954.1:c.820_826del
ENST00000645159.1:n.1911_1917del
ENST00000645550.1:n.387_393del
ENST00000645671.1:c.624_630del
ENST00000645730.1:c.521_527del
ENST00000646082.1:c.820_826del
ENST00000646571.1:c.1078_1084del
ENST00000647007.1:n.866_872del
ENST00000647133.1:c.674_680del
ENST00000315285.7:c.1174_1180del
ENST00000345662.5:c.1078_1084del
ENST00000615843.4:c.1174_1180del
ENST00000621856.1:c.916_922del
NM_014946.3:c.1174_1180del , LRG_714t1:c.1174_1180del
NM_199436.1:c.1078_1084del
XM_005264516.3:c.1171_1177del
XM_011533067.1:c.1174_1180del
NM_001363823.1:c.1171_1177del
NM_001363875.1:c.1075_1081del
XM_005264516.5:c.1171_1177del
XM_011533067.2:c.1174_1180del
XM_017004778.2:c.1078_1084del
NM_001363823.2:c.1171_1177del
NM_001363875.2:c.1075_1081del
NM_001377959.1:c.1078_1084del
NM_014946.4:c.1174_1180del
NM_199436.2:c.1078_1084del