Canonical Allele Identifier: CA425446637
Gene: SPAST HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.32352076T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32127007T>C , CM000664.2:g.32127007T>C GRCh38
NC_000002.11:g.32352076T>C , CM000664.1:g.32352076T>C GRCh37
NC_000002.10:g.32205580T>C NCBI36
NG_008730.1:g.68397T>C , LRG_714:g.68397T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.*818T>C ENSP00000515816.1:n.*818T>C
ENST00000315285.9:c.1158T>C MANE Select ENSP00000320885.3:p.Asn386=
ENST00000621856.2:c.1155T>C ENSP00000482496.2:p.Asn385=
ENST00000642281.1:c.983-9556T>C
ENST00000642455.1:c.1059T>C ENSP00000493827.1:p.Asn353=
ENST00000642751.1:c.932T>C
ENST00000642999.1:c.900T>C ENSP00000496589.1:p.Asn300=
ENST00000643327.1:c.317T>C
ENST00000643334.1:c.738T>C
ENST00000644408.1:c.1034T>C
ENST00000644954.1:c.804T>C ENSP00000494312.1:p.Asn268=
ENST00000645159.1:n.510T>C
ENST00000645550.1:n.371T>C
ENST00000645671.1:c.608T>C
ENST00000645730.1:c.505T>C
ENST00000646082.1:c.804T>C
ENST00000646571.1:c.1062T>C ENSP00000495015.1:p.Asn354=
ENST00000647007.1:n.850T>C
ENST00000647133.1:c.674-1401T>C
ENST00000315285.7:c.1158T>C ENSP00000320885.3:p.Asn386=
ENST00000345662.5:c.1062T>C ENSP00000340817.1:p.Asn354=
ENST00000615843.4:c.1158T>C ENSP00000480893.1:p.Asn386=
ENST00000621856.1:c.900T>C ENSP00000482496.1:p.Asn300=
NM_014946.3:c.1158T>C , LRG_714t1:c.1158T>C NP_055761.2:p.Asn386=
NM_199436.1:c.1062T>C NP_955468.1:p.Asn354=
XM_005264516.3:c.1155T>C XP_005264573.1:p.Asn385=
XM_011533067.1:c.1158T>C XP_011531369.1:p.Asn386=
NM_001363823.1:c.1155T>C NP_001350752.1:p.Asn385=
NM_001363875.1:c.1059T>C NP_001350804.1:p.Asn353=
XM_005264516.5:c.1155T>C XP_005264573.1:p.Asn385=
XM_011533067.2:c.1158T>C XP_011531369.1:p.Asn386=
XM_017004778.2:c.1062T>C XP_016860267.1:p.Asn354=
NM_001363823.2:c.1155T>C NP_001350752.1:p.Asn385=
NM_001363875.2:c.1059T>C NP_001350804.1:p.Asn353=
NM_001377959.1:c.1062T>C NP_001364888.1:p.Asn354=
NM_014946.4:c.1158T>C MANE Select NP_055761.2:p.Asn386=
NM_199436.2:c.1062T>C NP_955468.1:p.Asn354=