Canonical Allele Identifier: CA2699033104
Gene: SPAST HGNC NCBI

Linked Data

dbSNP Id: rs2148685233

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32063911_32063912insG , CM000664.2:g.32063911_32063912insG GRCh38
NC_000002.11:g.32288980_32288981insG , CM000664.1:g.32288980_32288981insG GRCh37
NC_000002.10:g.32142484_32142485insG NCBI36
NG_008730.1:g.5301_5302insG , LRG_714:g.5301_5302insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.80_81insG ENSP00000515816.1:p.Cys28LeufsTer20
ENST00000315285.9:c.80_81insG MANE Select ENSP00000320885.3:p.Cys28LeufsTer20
ENST00000621856.2:c.80_81insG ENSP00000482496.2:p.Cys28LeufsTer20
ENST00000642455.1:c.80_81insG ENSP00000493827.1:p.Cys28LeufsTer20
ENST00000646571.1:c.80_81insG ENSP00000495015.1:p.Cys28LeufsTer20
ENST00000315285.7:c.80_81insG ENSP00000320885.3:p.Cys28LeufsTer20
ENST00000345662.5:c.80_81insG ENSP00000340817.1:p.Cys28LeufsTer20
ENST00000615843.4:c.80_81insG ENSP00000480893.1:p.Cys28LeufsTer20
NM_014946.3:c.80_81insG , LRG_714t1:c.80_81insG NP_055761.2:p.Cys28LeufsTer20
NM_199436.1:c.80_81insG NP_955468.1:p.Cys28LeufsTer20
XM_005264516.3:c.80_81insG XP_005264573.1:p.Cys28LeufsTer20
XM_011533067.1:c.80_81insG XP_011531369.1:p.Cys28LeufsTer20
NM_001363823.1:c.80_81insG NP_001350752.1:p.Cys28LeufsTer20
NM_001363875.1:c.80_81insG NP_001350804.1:p.Cys28LeufsTer20
XM_005264516.5:c.80_81insG XP_005264573.1:p.Cys28LeufsTer20
XM_011533067.2:c.80_81insG XP_011531369.1:p.Cys28LeufsTer20
XM_017004778.2:c.80_81insG XP_016860267.1:p.Cys28LeufsTer20
NM_001363823.2:c.80_81insG NP_001350752.1:p.Cys28LeufsTer20
NM_001363875.2:c.80_81insG NP_001350804.1:p.Cys28LeufsTer20
NM_001377959.1:c.80_81insG NP_001364888.1:p.Cys28LeufsTer20
NM_014946.4:c.80_81insG MANE Select NP_055761.2:p.Cys28LeufsTer20
NM_199436.2:c.80_81insG NP_955468.1:p.Cys28LeufsTer20