Canonical Allele Identifier: CA346502100
Gene: SPAST HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32136618A>T , CM000664.2:g.32136618A>T GRCh38
NC_000002.11:g.32361687A>T , CM000664.1:g.32361687A>T GRCh37
NC_000002.10:g.32215191A>T NCBI36
NG_008730.1:g.78008A>T , LRG_714:g.78008A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000704289.1:c.*961A>T ENSP00000515816.1:n.*961A>T
ENST00000315285.9:c.1301A>T MANE Select ENSP00000320885.3:p.Gln434Leu
ENST00000621856.2:c.1298A>T ENSP00000482496.2:p.Gln433Leu
ENST00000642281.1:c.1038A>T
ENST00000642455.1:c.1202A>T ENSP00000493827.1:p.Gln401Leu
ENST00000642751.1:c.1075A>T
ENST00000642999.1:c.1043A>T ENSP00000496589.1:p.Gln348Leu
ENST00000643327.1:c.460A>T
ENST00000643334.1:c.881A>T
ENST00000644408.1:c.1177A>T
ENST00000644954.1:c.947A>T ENSP00000494312.1:p.Gln316Leu
ENST00000645159.1:n.2038A>T
ENST00000645671.1:c.751A>T
ENST00000645730.1:c.593-491A>T
ENST00000646082.1:c.947A>T
ENST00000646571.1:c.1205A>T ENSP00000495015.1:p.Gln402Leu
ENST00000647007.1:n.993A>T
ENST00000647133.1:c.801A>T
ENST00000315285.7:c.1301A>T ENSP00000320885.3:p.Gln434Leu
ENST00000345662.5:c.1205A>T ENSP00000340817.1:p.Gln402Leu
ENST00000615843.4:c.1301A>T ENSP00000480893.1:p.Gln434Leu
ENST00000621856.1:c.1043A>T ENSP00000482496.1:p.Gln348Leu
NM_014946.3:c.1301A>T , LRG_714t1:c.1301A>T NP_055761.2:p.Gln434Leu
NM_199436.1:c.1205A>T NP_955468.1:p.Gln402Leu
XM_005264516.3:c.1298A>T XP_005264573.1:p.Gln433Leu
XM_011533067.1:c.1301A>T XP_011531369.1:p.Gln434Leu
NM_001363823.1:c.1298A>T NP_001350752.1:p.Gln433Leu
NM_001363875.1:c.1202A>T NP_001350804.1:p.Gln401Leu
XM_005264516.5:c.1298A>T XP_005264573.1:p.Gln433Leu
XM_011533067.2:c.1301A>T XP_011531369.1:p.Gln434Leu
XM_017004778.2:c.1205A>T XP_016860267.1:p.Gln402Leu
NM_001363823.2:c.1298A>T NP_001350752.1:p.Gln433Leu
NM_001363875.2:c.1202A>T NP_001350804.1:p.Gln401Leu
NM_001377959.1:c.1205A>T NP_001364888.1:p.Gln402Leu
NM_014946.4:c.1301A>T MANE Select NP_055761.2:p.Gln434Leu
NM_199436.2:c.1205A>T NP_955468.1:p.Gln402Leu