Canonical Allele Identifier: CA1242461833
Gene: SPAST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32064243A= , CM000664.2:g.32064243A= GRCh38
NC_000002.11:g.32289312A= , CM000664.1:g.32289312A= GRCh37
NC_000002.10:g.32142816A= NCBI36
NG_008730.1:g.5633A= , LRG_714:g.5633A=

Transcript Alleles

HGVS Amino-acid change
ENST00000704289.1:c.412A= ENSP00000515816.1:p.Lys138=
ENST00000315285.9:c.412A= MANE Select ENSP00000320885.3:p.Lys138=
ENST00000621856.2:c.412A= ENSP00000482496.2:p.Lys138=
ENST00000642281.1:c.296A=
ENST00000642455.1:c.412A= ENSP00000493827.1:p.Lys138=
ENST00000642751.1:c.282A=
ENST00000642999.1:c.154A= ENSP00000496589.1:p.Lys52=
ENST00000644408.1:c.288A=
ENST00000644954.1:c.154A= ENSP00000494312.1:p.Lys52=
ENST00000645400.1:c.253A= ENSP00000496306.1:p.Lys85=
ENST00000645671.1:c.33A=
ENST00000646082.1:c.246A=
ENST00000646571.1:c.412A= ENSP00000495015.1:p.Lys138=
ENST00000315285.7:c.412A= ENSP00000320885.3:p.Lys138=
ENST00000345662.5:c.412A= ENSP00000340817.1:p.Lys138=
ENST00000615843.4:c.412A= ENSP00000480893.1:p.Lys138=
ENST00000621856.1:c.154A= ENSP00000482496.1:p.Lys52=
NM_014946.3:c.412A= , LRG_714t1:c.412A= NP_055761.2:p.Lys138=
NM_199436.1:c.412A= NP_955468.1:p.Lys138=
XM_005264516.3:c.412A= XP_005264573.1:p.Lys138=
XM_011533067.1:c.412A= XP_011531369.1:p.Lys138=
NM_001363823.1:c.412A= NP_001350752.1:p.Lys138=
NM_001363875.1:c.412A= NP_001350804.1:p.Lys138=
XM_005264516.5:c.412A= XP_005264573.1:p.Lys138=
XM_011533067.2:c.412A= XP_011531369.1:p.Lys138=
XM_017004778.2:c.412A= XP_016860267.1:p.Lys138=
NM_001363823.2:c.412A= NP_001350752.1:p.Lys138=
NM_001363875.2:c.412A= NP_001350804.1:p.Lys138=
NM_001377959.1:c.412A= NP_001364888.1:p.Lys138=
NM_014946.4:c.412A= MANE Select NP_055761.2:p.Lys138=
NM_199436.2:c.412A= NP_955468.1:p.Lys138=