Canonical Allele Identifier: CA2658518972
Gene: SPAST HGNC NCBI

Linked Data

gnomAD v4: 2-32063824-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32063824A>G , CM000664.2:g.32063824A>G GRCh38
NC_000002.11:g.32288893A>G , CM000664.1:g.32288893A>G GRCh37
NC_000002.10:g.32142397A>G NCBI36
NG_008730.1:g.5214A>G , LRG_714:g.5214A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.-8A>G ENSP00000515816.1:n.-8A>G
ENST00000315285.9:c.-8A>G MANE Select ENSP00000320885.3:n.-8A>G
ENST00000621856.2:c.-8A>G ENSP00000482496.2:n.-8A>G
ENST00000646571.1:c.-8A>G ENSP00000495015.1:n.-8A>G
ENST00000315285.7:c.-8A>G ENSP00000320885.3:n.-8A>G
ENST00000345662.5:c.-8A>G ENSP00000340817.1:n.-8A>G
ENST00000615843.4:c.-8A>G ENSP00000480893.1:n.-8A>G
NM_014946.3:c.-8A>G , LRG_714t1:c.-8A>G NP_055761.2:n.-8A>G
NM_199436.1:c.-8A>G NP_955468.1:n.-8A>G
XM_005264516.3:c.-8A>G XP_005264573.1:n.-8A>G
XM_011533067.1:c.-8A>G XP_011531369.1:n.-8A>G
NM_001363823.1:c.-8A>G NP_001350752.1:n.-8A>G
NM_001363875.1:c.-8A>G NP_001350804.1:n.-8A>G
XM_011533067.2:c.-8A>G XP_011531369.1:n.-8A>G
XM_017004778.2:c.-8A>G XP_016860267.1:n.-8A>G
NM_001363823.2:c.-8A>G NP_001350752.1:n.-8A>G
NM_001363875.2:c.-8A>G NP_001350804.1:n.-8A>G
NM_001377959.1:c.-8A>G NP_001364888.1:n.-8A>G
NM_014946.4:c.-8A>G MANE Select NP_055761.2:n.-8A>G
NM_199436.2:c.-8A>G NP_955468.1:n.-8A>G