Canonical Allele Identifier: CA1242504477
Gene: SPAST HGNC NCBI

Linked Data

dbSNP Id: rs1679729036

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32141824del , CM000664.2:g.32141824del GRCh38
NC_000002.11:g.32366893del , CM000664.1:g.32366893del GRCh37
NC_000002.10:g.32220397del NCBI36
NG_008730.1:g.83214del , LRG_714:g.83214del

Transcript Alleles

HGVS Amino-acid change
ENST00000704289.1:c.*1154-80del ENSP00000515816.1:n.*1154-80del
ENST00000315285.9:c.1494-80del MANE Select ENSP00000320885.3:n.1494-80del
ENST00000621856.2:c.1491-80del ENSP00000482496.2:n.1491-80del
ENST00000642281.1:c.1231-80del
ENST00000642455.1:c.1395-80del ENSP00000493827.1:n.1395-80del
ENST00000642751.1:c.1268-80del
ENST00000642999.1:c.1236-80del ENSP00000496589.1:n.1236-80del
ENST00000643327.1:c.561-80del
ENST00000643334.1:c.1074-80del
ENST00000644408.1:c.1370-80del
ENST00000644954.1:c.1140-80del ENSP00000494312.1:n.1140-80del
ENST00000645159.1:n.2231-80del
ENST00000645671.1:c.944-80del
ENST00000645730.1:c.673-80del
ENST00000646082.1:c.1140-80del
ENST00000646571.1:c.1398-80del ENSP00000495015.1:n.1398-80del
ENST00000647007.1:n.1186-80del
ENST00000647133.1:c.994-80del
ENST00000315285.7:c.1494-80del ENSP00000320885.3:n.1494-80del
ENST00000345662.5:c.1398-80del ENSP00000340817.1:n.1398-80del
ENST00000615843.4:c.1494-80del ENSP00000480893.1:n.1494-80del
ENST00000621856.1:c.1236-80del ENSP00000482496.1:n.1236-80del
NM_014946.3:c.1494-80del , LRG_714t1:c.1494-80del NP_055761.2:n.1494-80del
NM_199436.1:c.1398-80del NP_955468.1:n.1398-80del
XM_005264516.3:c.1491-80del XP_005264573.1:n.1491-80del
XM_011533067.1:c.1494-80del XP_011531369.1:n.1494-80del
NM_001363823.1:c.1491-80del NP_001350752.1:n.1491-80del
NM_001363875.1:c.1395-80del NP_001350804.1:n.1395-80del
XM_005264516.5:c.1491-80del XP_005264573.1:n.1491-80del
XM_011533067.2:c.1494-80del XP_011531369.1:n.1494-80del
XM_017004778.2:c.1398-80del XP_016860267.1:n.1398-80del
NM_001363823.2:c.1491-80del NP_001350752.1:n.1491-80del
NM_001363875.2:c.1395-80del NP_001350804.1:n.1395-80del
NM_001377959.1:c.1398-80del NP_001364888.1:n.1398-80del
NM_014946.4:c.1494-80del MANE Select NP_055761.2:n.1494-80del
NM_199436.2:c.1398-80del NP_955468.1:n.1398-80del