Canonical Allele Identifier: CA425446884
Gene: SPAST HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.32353488A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32128419A>T , CM000664.2:g.32128419A>T GRCh38
NC_000002.11:g.32353488A>T , CM000664.1:g.32353488A>T GRCh37
NC_000002.10:g.32206992A>T NCBI36
NG_008730.1:g.69809A>T , LRG_714:g.69809A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.*845A>T ENSP00000515816.1:n.*845A>T
ENST00000315285.9:c.1185A>T MANE Select ENSP00000320885.3:p.Val395=
ENST00000621856.2:c.1182A>T ENSP00000482496.2:p.Val394=
ENST00000642281.1:c.983-8144A>T
ENST00000642455.1:c.1086A>T ENSP00000493827.1:p.Val362=
ENST00000642751.1:c.959A>T
ENST00000642999.1:c.927A>T ENSP00000496589.1:p.Val309=
ENST00000643327.1:c.344A>T
ENST00000643334.1:c.765A>T
ENST00000644408.1:c.1061A>T
ENST00000644954.1:c.831A>T ENSP00000494312.1:p.Val277=
ENST00000645159.1:n.1922A>T
ENST00000645550.1:n.398A>T
ENST00000645671.1:c.635A>T
ENST00000645730.1:c.532A>T
ENST00000646082.1:c.831A>T
ENST00000646571.1:c.1089A>T ENSP00000495015.1:p.Val363=
ENST00000647007.1:n.877A>T
ENST00000647133.1:c.685A>T
ENST00000315285.7:c.1185A>T ENSP00000320885.3:p.Val395=
ENST00000345662.5:c.1089A>T ENSP00000340817.1:p.Val363=
ENST00000615843.4:c.1185A>T ENSP00000480893.1:p.Val395=
ENST00000621856.1:c.927A>T ENSP00000482496.1:p.Val309=
NM_014946.3:c.1185A>T , LRG_714t1:c.1185A>T NP_055761.2:p.Val395=
NM_199436.1:c.1089A>T NP_955468.1:p.Val363=
XM_005264516.3:c.1182A>T XP_005264573.1:p.Val394=
XM_011533067.1:c.1185A>T XP_011531369.1:p.Val395=
NM_001363823.1:c.1182A>T NP_001350752.1:p.Val394=
NM_001363875.1:c.1086A>T NP_001350804.1:p.Val362=
XM_005264516.5:c.1182A>T XP_005264573.1:p.Val394=
XM_011533067.2:c.1185A>T XP_011531369.1:p.Val395=
XM_017004778.2:c.1089A>T XP_016860267.1:p.Val363=
NM_001363823.2:c.1182A>T NP_001350752.1:p.Val394=
NM_001363875.2:c.1086A>T NP_001350804.1:p.Val362=
NM_001377959.1:c.1089A>T NP_001364888.1:p.Val363=
NM_014946.4:c.1185A>T MANE Select NP_055761.2:p.Val395=
NM_199436.2:c.1089A>T NP_955468.1:p.Val363=