Canonical Allele Identifier: CA346504366
Gene: SPAST HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32147244A>T , CM000664.2:g.32147244A>T GRCh38
NC_000002.11:g.32372313A>T , CM000664.1:g.32372313A>T GRCh37
NC_000002.10:g.32225817A>T NCBI36
NG_008730.1:g.88634A>T , LRG_714:g.88634A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.*1374A>T ENSP00000515816.1:n.*1374A>T
ENST00000315285.9:c.1714A>T MANE Select ENSP00000320885.3:p.Met572Leu
ENST00000621856.2:c.1711A>T ENSP00000482496.2:p.Met571Leu
ENST00000642281.1:c.1451A>T
ENST00000642455.1:c.1615A>T ENSP00000493827.1:p.Met539Leu
ENST00000642751.1:c.1417A>T
ENST00000642999.1:c.1456A>T ENSP00000496589.1:p.Met486Leu
ENST00000643334.1:c.1294A>T
ENST00000644408.1:c.1613A>T
ENST00000644954.1:c.1360A>T ENSP00000494312.1:p.Met454Leu
ENST00000645159.1:n.2451A>T
ENST00000645671.1:c.1093A>T
ENST00000645730.1:c.893A>T
ENST00000646082.1:c.1360A>T
ENST00000646571.1:c.1618A>T ENSP00000495015.1:p.Met540Leu
ENST00000647007.1:n.1406A>T
ENST00000647133.1:c.1214A>T
ENST00000315285.7:c.1714A>T ENSP00000320885.3:p.Met572Leu
ENST00000345662.5:c.1618A>T ENSP00000340817.1:p.Met540Leu
ENST00000615843.4:c.1714A>T ENSP00000480893.1:p.Met572Leu
ENST00000621856.1:c.1456A>T ENSP00000482496.1:p.Met486Leu
NM_014946.3:c.1714A>T , LRG_714t1:c.1714A>T NP_055761.2:p.Met572Leu
NM_199436.1:c.1618A>T NP_955468.1:p.Met540Leu
XM_005264516.3:c.1711A>T XP_005264573.1:p.Met571Leu
XM_011533067.1:c.1643A>T XP_011531369.1:p.Tyr548Phe
NM_001363823.1:c.1711A>T NP_001350752.1:p.Met571Leu
NM_001363875.1:c.1615A>T NP_001350804.1:p.Met539Leu
XM_005264516.5:c.1711A>T XP_005264573.1:p.Met571Leu
XM_011533067.2:c.1643A>T XP_011531369.1:p.Tyr548Phe
XM_017004778.2:c.1547A>T XP_016860267.1:p.Tyr516Phe
NM_001363823.2:c.1711A>T NP_001350752.1:p.Met571Leu
NM_001363875.2:c.1615A>T NP_001350804.1:p.Met539Leu
NM_001377959.1:c.1547A>T NP_001364888.1:p.Tyr516Phe
NM_014946.4:c.1714A>T MANE Select NP_055761.2:p.Met572Leu
NM_199436.2:c.1618A>T NP_955468.1:p.Met540Leu