Canonical Allele Identifier: CA1242501912
Gene: SPAST HGNC NCBI

Linked Data

dbSNP Id: rs1679561036
gnomAD v4: 2-32137020-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32137020C>T , CM000664.2:g.32137020C>T GRCh38
NC_000002.11:g.32362089C>T , CM000664.1:g.32362089C>T GRCh37
NC_000002.10:g.32215593C>T NCBI36
NG_008730.1:g.78410C>T , LRG_714:g.78410C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.*1073+52C>T ENSP00000515816.1:n.*1073+52C>T
ENST00000315285.9:c.1413+52C>T MANE Select ENSP00000320885.3:n.1413+52C>T
ENST00000621856.2:c.1410+52C>T ENSP00000482496.2:n.1410+52C>T
ENST00000642281.1:c.1150+52C>T
ENST00000642455.1:c.1314+52C>T ENSP00000493827.1:n.1314+52C>T
ENST00000642751.1:c.1187+52C>T
ENST00000642999.1:c.1155+52C>T ENSP00000496589.1:n.1155+52C>T
ENST00000643327.1:c.481-89C>T
ENST00000643334.1:c.993+52C>T
ENST00000644408.1:c.1289+52C>T
ENST00000644954.1:c.1059+52C>T ENSP00000494312.1:n.1059+52C>T
ENST00000645159.1:n.2150+52C>T
ENST00000645671.1:c.863+52C>T
ENST00000645730.1:c.593-89C>T
ENST00000646082.1:c.1059+52C>T
ENST00000646571.1:c.1317+52C>T ENSP00000495015.1:n.1317+52C>T
ENST00000647007.1:n.1105+52C>T
ENST00000647133.1:c.913+52C>T
ENST00000315285.7:c.1413+52C>T ENSP00000320885.3:n.1413+52C>T
ENST00000345662.5:c.1317+52C>T ENSP00000340817.1:n.1317+52C>T
ENST00000615843.4:c.1413+52C>T ENSP00000480893.1:n.1413+52C>T
ENST00000621856.1:c.1155+52C>T ENSP00000482496.1:n.1155+52C>T
NM_014946.3:c.1413+52C>T , LRG_714t1:c.1413+52C>T NP_055761.2:n.1413+52C>T
NM_199436.1:c.1317+52C>T NP_955468.1:n.1317+52C>T
XM_005264516.3:c.1410+52C>T XP_005264573.1:n.1410+52C>T
XM_011533067.1:c.1413+52C>T XP_011531369.1:n.1413+52C>T
NM_001363823.1:c.1410+52C>T NP_001350752.1:n.1410+52C>T
NM_001363875.1:c.1314+52C>T NP_001350804.1:n.1314+52C>T
XM_005264516.5:c.1410+52C>T XP_005264573.1:n.1410+52C>T
XM_011533067.2:c.1413+52C>T XP_011531369.1:n.1413+52C>T
XM_017004778.2:c.1317+52C>T XP_016860267.1:n.1317+52C>T
NM_001363823.2:c.1410+52C>T NP_001350752.1:n.1410+52C>T
NM_001363875.2:c.1314+52C>T NP_001350804.1:n.1314+52C>T
NM_001377959.1:c.1317+52C>T NP_001364888.1:n.1317+52C>T
NM_014946.4:c.1413+52C>T MANE Select NP_055761.2:n.1413+52C>T
NM_199436.2:c.1317+52C>T NP_955468.1:n.1317+52C>T