Canonical Allele Identifier: CA2699033096
Gene: SPAST HGNC NCBI

Linked Data

dbSNP Id: rs2148685230

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32063912_32063915del , CM000664.2:g.32063912_32063915del GRCh38
NC_000002.11:g.32288981_32288984del , CM000664.1:g.32288981_32288984del GRCh37
NC_000002.10:g.32142485_32142488del NCBI36
NG_008730.1:g.5302_5305del , LRG_714:g.5302_5305del

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.81_84del ENSP00000515816.1:p.Cys28TrpfsTer?
ENST00000315285.9:c.81_84del MANE Select ENSP00000320885.3:p.Cys28TrpfsTer?
ENST00000621856.2:c.81_84del ENSP00000482496.2:p.Cys28TrpfsTer?
ENST00000642455.1:c.81_84del ENSP00000493827.1:p.Cys28TrpfsTer?
ENST00000646571.1:c.81_84del ENSP00000495015.1:p.Cys28TrpfsTer?
ENST00000315285.7:c.81_84del ENSP00000320885.3:p.Cys28TrpfsTer?
ENST00000345662.5:c.81_84del ENSP00000340817.1:p.Cys28TrpfsTer?
ENST00000615843.4:c.81_84del ENSP00000480893.1:p.Cys28TrpfsTer?
NM_014946.3:c.81_84del , LRG_714t1:c.81_84del NP_055761.2:p.Cys28TrpfsTer?
NM_199436.1:c.81_84del NP_955468.1:p.Cys28TrpfsTer?
XM_005264516.3:c.81_84del XP_005264573.1:p.Cys28TrpfsTer?
XM_011533067.1:c.81_84del XP_011531369.1:p.Cys28TrpfsTer?
NM_001363823.1:c.81_84del NP_001350752.1:p.Cys28TrpfsTer?
NM_001363875.1:c.81_84del NP_001350804.1:p.Cys28TrpfsTer?
XM_005264516.5:c.81_84del XP_005264573.1:p.Cys28TrpfsTer?
XM_011533067.2:c.81_84del XP_011531369.1:p.Cys28TrpfsTer?
XM_017004778.2:c.81_84del XP_016860267.1:p.Cys28TrpfsTer?
NM_001363823.2:c.81_84del NP_001350752.1:p.Cys28TrpfsTer?
NM_001363875.2:c.81_84del NP_001350804.1:p.Cys28TrpfsTer?
NM_001377959.1:c.81_84del NP_001364888.1:p.Cys28TrpfsTer?
NM_014946.4:c.81_84del MANE Select NP_055761.2:p.Cys28TrpfsTer?
NM_199436.2:c.81_84del NP_955468.1:p.Cys28TrpfsTer?