Canonical Allele Identifier: CA346502106
Gene: SPAST HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32136621C>G , CM000664.2:g.32136621C>G GRCh38
NC_000002.11:g.32361690C>G , CM000664.1:g.32361690C>G GRCh37
NC_000002.10:g.32215194C>G NCBI36
NG_008730.1:g.78011C>G , LRG_714:g.78011C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.*964C>G ENSP00000515816.1:n.*964C>G
ENST00000315285.9:c.1304C>G MANE Select ENSP00000320885.3:p.Pro435Arg
ENST00000621856.2:c.1301C>G ENSP00000482496.2:p.Pro434Arg
ENST00000642281.1:c.1041C>G
ENST00000642455.1:c.1205C>G ENSP00000493827.1:p.Pro402Arg
ENST00000642751.1:c.1078C>G
ENST00000642999.1:c.1046C>G ENSP00000496589.1:p.Pro349Arg
ENST00000643327.1:c.463C>G
ENST00000643334.1:c.884C>G
ENST00000644408.1:c.1180C>G
ENST00000644954.1:c.950C>G ENSP00000494312.1:p.Pro317Arg
ENST00000645159.1:n.2041C>G
ENST00000645671.1:c.754C>G
ENST00000645730.1:c.593-488C>G
ENST00000646082.1:c.950C>G
ENST00000646571.1:c.1208C>G ENSP00000495015.1:p.Pro403Arg
ENST00000647007.1:n.996C>G
ENST00000647133.1:c.804C>G
ENST00000315285.7:c.1304C>G ENSP00000320885.3:p.Pro435Arg
ENST00000345662.5:c.1208C>G ENSP00000340817.1:p.Pro403Arg
ENST00000615843.4:c.1304C>G ENSP00000480893.1:p.Pro435Arg
ENST00000621856.1:c.1046C>G ENSP00000482496.1:p.Pro349Arg
NM_014946.3:c.1304C>G , LRG_714t1:c.1304C>G NP_055761.2:p.Pro435Arg
NM_199436.1:c.1208C>G NP_955468.1:p.Pro403Arg
XM_005264516.3:c.1301C>G XP_005264573.1:p.Pro434Arg
XM_011533067.1:c.1304C>G XP_011531369.1:p.Pro435Arg
NM_001363823.1:c.1301C>G NP_001350752.1:p.Pro434Arg
NM_001363875.1:c.1205C>G NP_001350804.1:p.Pro402Arg
XM_005264516.5:c.1301C>G XP_005264573.1:p.Pro434Arg
XM_011533067.2:c.1304C>G XP_011531369.1:p.Pro435Arg
XM_017004778.2:c.1208C>G XP_016860267.1:p.Pro403Arg
NM_001363823.2:c.1301C>G NP_001350752.1:p.Pro434Arg
NM_001363875.2:c.1205C>G NP_001350804.1:p.Pro402Arg
NM_001377959.1:c.1208C>G NP_001364888.1:p.Pro403Arg
NM_014946.4:c.1304C>G MANE Select NP_055761.2:p.Pro435Arg
NM_199436.2:c.1208C>G NP_955468.1:p.Pro403Arg