Canonical Allele Identifier: CA2658518937
Gene: SPAST HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32063790_32063791insAA , CM000664.2:g.32063790_32063791insAA GRCh38
NC_000002.11:g.32288859_32288860insAA , CM000664.1:g.32288859_32288860insAA GRCh37
NC_000002.10:g.32142363_32142364insAA NCBI36
NG_008730.1:g.5180_5181insAA , LRG_714:g.5180_5181insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.-42_-41insAA ENSP00000515816.1:n.-42_-41insAA
ENST00000315285.9:c.-42_-41insAA MANE Select ENSP00000320885.3:n.-42_-41insAA
ENST00000621856.2:c.-42_-41insAA ENSP00000482496.2:n.-42_-41insAA
ENST00000646571.1:c.-42_-41insAA ENSP00000495015.1:n.-42_-41insAA
ENST00000315285.7:c.-42_-41insAA ENSP00000320885.3:n.-42_-41insAA
ENST00000345662.5:c.-42_-41insAA ENSP00000340817.1:n.-42_-41insAA
ENST00000615843.4:c.-42_-41insAA ENSP00000480893.1:n.-42_-41insAA
NM_014946.3:c.-42_-41insAA , LRG_714t1:c.-42_-41insAA NP_055761.2:n.-42_-41insAA
NM_199436.1:c.-42_-41insAA NP_955468.1:n.-42_-41insAA
XM_005264516.3:c.-42_-41insAA XP_005264573.1:n.-42_-41insAA
XM_011533067.1:c.-42_-41insAA XP_011531369.1:n.-42_-41insAA
NM_001363823.1:c.-42_-41insAA NP_001350752.1:n.-42_-41insAA
NM_001363875.1:c.-42_-41insAA NP_001350804.1:n.-42_-41insAA
XM_011533067.2:c.-42_-41insAA XP_011531369.1:n.-42_-41insAA
XM_017004778.2:c.-42_-41insAA XP_016860267.1:n.-42_-41insAA
NM_001363823.2:c.-42_-41insAA NP_001350752.1:n.-42_-41insAA
NM_001363875.2:c.-42_-41insAA NP_001350804.1:n.-42_-41insAA
NM_001377959.1:c.-42_-41insAA NP_001364888.1:n.-42_-41insAA
NM_014946.4:c.-42_-41insAA MANE Select NP_055761.2:n.-42_-41insAA
NM_199436.2:c.-42_-41insAA NP_955468.1:n.-42_-41insAA