Canonical Allele Identifier: CA346502045
Gene: SPAST HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32136591C>G , CM000664.2:g.32136591C>G GRCh38
NC_000002.11:g.32361660C>G , CM000664.1:g.32361660C>G GRCh37
NC_000002.10:g.32215164C>G NCBI36
NG_008730.1:g.77981C>G , LRG_714:g.77981C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.*934C>G ENSP00000515816.1:n.*934C>G
ENST00000315285.9:c.1274C>G MANE Select ENSP00000320885.3:p.Ala425Gly
ENST00000621856.2:c.1271C>G ENSP00000482496.2:p.Ala424Gly
ENST00000642281.1:c.1011C>G
ENST00000642455.1:c.1175C>G ENSP00000493827.1:p.Ala392Gly
ENST00000642751.1:c.1048C>G
ENST00000642999.1:c.1016C>G ENSP00000496589.1:p.Ala339Gly
ENST00000643327.1:c.433C>G
ENST00000643334.1:c.854C>G
ENST00000644408.1:c.1150C>G
ENST00000644954.1:c.920C>G ENSP00000494312.1:p.Ala307Gly
ENST00000645159.1:n.2011C>G
ENST00000645671.1:c.724C>G
ENST00000645730.1:c.593-518C>G
ENST00000646082.1:c.920C>G
ENST00000646571.1:c.1178C>G ENSP00000495015.1:p.Ala393Gly
ENST00000647007.1:n.966C>G
ENST00000647133.1:c.774C>G
ENST00000315285.7:c.1274C>G ENSP00000320885.3:p.Ala425Gly
ENST00000345662.5:c.1178C>G ENSP00000340817.1:p.Ala393Gly
ENST00000615843.4:c.1274C>G ENSP00000480893.1:p.Ala425Gly
ENST00000621856.1:c.1016C>G ENSP00000482496.1:p.Ala339Gly
NM_014946.3:c.1274C>G , LRG_714t1:c.1274C>G NP_055761.2:p.Ala425Gly
NM_199436.1:c.1178C>G NP_955468.1:p.Ala393Gly
XM_005264516.3:c.1271C>G XP_005264573.1:p.Ala424Gly
XM_011533067.1:c.1274C>G XP_011531369.1:p.Ala425Gly
NM_001363823.1:c.1271C>G NP_001350752.1:p.Ala424Gly
NM_001363875.1:c.1175C>G NP_001350804.1:p.Ala392Gly
XM_005264516.5:c.1271C>G XP_005264573.1:p.Ala424Gly
XM_011533067.2:c.1274C>G XP_011531369.1:p.Ala425Gly
XM_017004778.2:c.1178C>G XP_016860267.1:p.Ala393Gly
NM_001363823.2:c.1271C>G NP_001350752.1:p.Ala424Gly
NM_001363875.2:c.1175C>G NP_001350804.1:p.Ala392Gly
NM_001377959.1:c.1178C>G NP_001364888.1:p.Ala393Gly
NM_014946.4:c.1274C>G MANE Select NP_055761.2:p.Ala425Gly
NM_199436.2:c.1178C>G NP_955468.1:p.Ala393Gly