Canonical Allele Identifier: CA645523266
Gene: SPAST HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32136639dup , CM000664.2:g.32136639dup GRCh38
NC_000002.11:g.32361708dup , CM000664.1:g.32361708dup GRCh37
NC_000002.10:g.32215212dup NCBI36
NG_008730.1:g.78029dup , LRG_714:g.78029dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.*981+1dup
ENST00000315285.9:c.1321+1dup
ENST00000621856.2:c.1318+1dup
ENST00000642281.1:c.1058+1dup
ENST00000642455.1:c.1222+1dup
ENST00000642751.1:c.1095+1dup
ENST00000642999.1:c.1063+1dup
ENST00000643327.1:c.480+1dup
ENST00000643334.1:c.901+1dup
ENST00000644408.1:c.1197+1dup
ENST00000644954.1:c.967+1dup
ENST00000645159.1:n.2058+1dup
ENST00000645671.1:c.771+1dup
ENST00000645730.1:c.593-470dup
ENST00000646082.1:c.967+1dup
ENST00000646571.1:c.1225+1dup
ENST00000647007.1:n.1013+1dup
ENST00000647133.1:c.821+1dup
ENST00000315285.7:c.1321+1dup
ENST00000345662.5:c.1225+1dup
ENST00000615843.4:c.1321+1dup
ENST00000621856.1:c.1063+1dup
NM_014946.3:c.1321+1dup , LRG_714t1:c.1321+1dup
NM_199436.1:c.1225+1dup
XM_005264516.3:c.1318+1dup
XM_011533067.1:c.1321+1dup
NM_001363823.1:c.1318+1dup
NM_001363875.1:c.1222+1dup
XM_005264516.5:c.1318+1dup
XM_011533067.2:c.1321+1dup
XM_017004778.2:c.1225+1dup
NM_001363823.2:c.1318+1dup
NM_001363875.2:c.1222+1dup
NM_001377959.1:c.1225+1dup
NM_014946.4:c.1321+1dup
NM_199436.2:c.1225+1dup