Canonical Allele Identifier: CA346502081
Gene: SPAST HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32136611G>A , CM000664.2:g.32136611G>A GRCh38
NC_000002.11:g.32361680G>A , CM000664.1:g.32361680G>A GRCh37
NC_000002.10:g.32215184G>A NCBI36
NG_008730.1:g.78001G>A , LRG_714:g.78001G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000704289.1:c.*954G>A ENSP00000515816.1:n.*954G>A
ENST00000315285.9:c.1294G>A MANE Select ENSP00000320885.3:p.Glu432Lys
ENST00000621856.2:c.1291G>A ENSP00000482496.2:p.Glu431Lys
ENST00000642281.1:c.1031G>A
ENST00000642455.1:c.1195G>A ENSP00000493827.1:p.Glu399Lys
ENST00000642751.1:c.1068G>A
ENST00000642999.1:c.1036G>A ENSP00000496589.1:p.Glu346Lys
ENST00000643327.1:c.453G>A
ENST00000643334.1:c.874G>A
ENST00000644408.1:c.1170G>A
ENST00000644954.1:c.940G>A ENSP00000494312.1:p.Glu314Lys
ENST00000645159.1:n.2031G>A
ENST00000645671.1:c.744G>A
ENST00000645730.1:c.593-498G>A
ENST00000646082.1:c.940G>A
ENST00000646571.1:c.1198G>A ENSP00000495015.1:p.Glu400Lys
ENST00000647007.1:n.986G>A
ENST00000647133.1:c.794G>A
ENST00000315285.7:c.1294G>A ENSP00000320885.3:p.Glu432Lys
ENST00000345662.5:c.1198G>A ENSP00000340817.1:p.Glu400Lys
ENST00000615843.4:c.1294G>A ENSP00000480893.1:p.Glu432Lys
ENST00000621856.1:c.1036G>A ENSP00000482496.1:p.Glu346Lys
NM_014946.3:c.1294G>A , LRG_714t1:c.1294G>A NP_055761.2:p.Glu432Lys
NM_199436.1:c.1198G>A NP_955468.1:p.Glu400Lys
XM_005264516.3:c.1291G>A XP_005264573.1:p.Glu431Lys
XM_011533067.1:c.1294G>A XP_011531369.1:p.Glu432Lys
NM_001363823.1:c.1291G>A NP_001350752.1:p.Glu431Lys
NM_001363875.1:c.1195G>A NP_001350804.1:p.Glu399Lys
XM_005264516.5:c.1291G>A XP_005264573.1:p.Glu431Lys
XM_011533067.2:c.1294G>A XP_011531369.1:p.Glu432Lys
XM_017004778.2:c.1198G>A XP_016860267.1:p.Glu400Lys
NM_001363823.2:c.1291G>A NP_001350752.1:p.Glu431Lys
NM_001363875.2:c.1195G>A NP_001350804.1:p.Glu399Lys
NM_001377959.1:c.1198G>A NP_001364888.1:p.Glu400Lys
NM_014946.4:c.1294G>A MANE Select NP_055761.2:p.Glu432Lys
NM_199436.2:c.1198G>A NP_955468.1:p.Glu400Lys