Canonical Allele Identifier: CA346603584
Gene: SPAST HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32089593T>G , CM000664.2:g.32089593T>G GRCh38
NC_000002.11:g.32314662T>G , CM000664.1:g.32314662T>G GRCh37
NC_000002.10:g.32168166T>G NCBI36
NG_008730.1:g.30983T>G , LRG_714:g.30983T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000704289.1:c.*234T>G ENSP00000515816.1:n.*234T>G
ENST00000315285.9:c.574T>G MANE Select ENSP00000320885.3:p.Leu192Val
ENST00000621856.2:c.571T>G ENSP00000482496.2:p.Leu191Val
ENST00000642281.1:c.458T>G
ENST00000642455.1:c.571T>G ENSP00000493827.1:p.Leu191Val
ENST00000642751.1:c.444T>G
ENST00000642999.1:c.316T>G ENSP00000496589.1:p.Leu106Val
ENST00000643334.1:c.159T>G
ENST00000644408.1:c.450T>G
ENST00000644954.1:c.316T>G ENSP00000494312.1:p.Leu106Val
ENST00000645400.1:c.530T>G ENSP00000496306.1:n.530T>G
ENST00000645671.1:c.37-9203T>G
ENST00000646082.1:c.408T>G
ENST00000646571.1:c.574T>G ENSP00000495015.1:p.Leu192Val
ENST00000647007.1:n.271T>G
ENST00000647133.1:c.149T>G
ENST00000315285.7:c.574T>G ENSP00000320885.3:p.Leu192Val
ENST00000345662.5:c.574T>G ENSP00000340817.1:p.Leu192Val
ENST00000615843.4:c.574T>G ENSP00000480893.1:p.Leu192Val
ENST00000621856.1:c.316T>G ENSP00000482496.1:p.Leu106Val
NM_014946.3:c.574T>G , LRG_714t1:c.574T>G NP_055761.2:p.Leu192Val
NM_199436.1:c.574T>G NP_955468.1:p.Leu192Val
XM_005264516.3:c.571T>G XP_005264573.1:p.Leu191Val
XM_011533067.1:c.574T>G XP_011531369.1:p.Leu192Val
NM_001363823.1:c.571T>G NP_001350752.1:p.Leu191Val
NM_001363875.1:c.571T>G NP_001350804.1:p.Leu191Val
XM_005264516.5:c.571T>G XP_005264573.1:p.Leu191Val
XM_011533067.2:c.574T>G XP_011531369.1:p.Leu192Val
XM_017004778.2:c.574T>G XP_016860267.1:p.Leu192Val
NM_001363823.2:c.571T>G NP_001350752.1:p.Leu191Val
NM_001363875.2:c.571T>G NP_001350804.1:p.Leu191Val
NM_001377959.1:c.574T>G NP_001364888.1:p.Leu192Val
NM_014946.4:c.574T>G MANE Select NP_055761.2:p.Leu192Val
NM_199436.2:c.574T>G NP_955468.1:p.Leu192Val