Canonical Allele Identifier: CA425446571
Gene: SPAST HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.32352040T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32126971T>C , CM000664.2:g.32126971T>C GRCh38
NC_000002.11:g.32352040T>C , CM000664.1:g.32352040T>C GRCh37
NC_000002.10:g.32205544T>C NCBI36
NG_008730.1:g.68361T>C , LRG_714:g.68361T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.*782T>C ENSP00000515816.1:n.*782T>C
ENST00000315285.9:c.1122T>C MANE Select ENSP00000320885.3:p.Pro374=
ENST00000621856.2:c.1119T>C ENSP00000482496.2:p.Pro373=
ENST00000642281.1:c.983-9592T>C
ENST00000642455.1:c.1023T>C ENSP00000493827.1:p.Pro341=
ENST00000642751.1:c.896T>C
ENST00000642999.1:c.864T>C ENSP00000496589.1:p.Pro288=
ENST00000643327.1:c.281T>C
ENST00000643334.1:c.702T>C
ENST00000644408.1:c.998T>C
ENST00000644954.1:c.768T>C ENSP00000494312.1:p.Pro256=
ENST00000645159.1:n.474T>C
ENST00000645550.1:n.335T>C
ENST00000645671.1:c.572T>C
ENST00000645730.1:c.469T>C
ENST00000646082.1:c.768T>C
ENST00000646571.1:c.1026T>C ENSP00000495015.1:p.Pro342=
ENST00000647007.1:n.814T>C
ENST00000647133.1:c.674-1437T>C
ENST00000315285.7:c.1122T>C ENSP00000320885.3:p.Pro374=
ENST00000345662.5:c.1026T>C ENSP00000340817.1:p.Pro342=
ENST00000615843.4:c.1122T>C ENSP00000480893.1:p.Pro374=
ENST00000621856.1:c.864T>C ENSP00000482496.1:p.Pro288=
NM_014946.3:c.1122T>C , LRG_714t1:c.1122T>C NP_055761.2:p.Pro374=
NM_199436.1:c.1026T>C NP_955468.1:p.Pro342=
XM_005264516.3:c.1119T>C XP_005264573.1:p.Pro373=
XM_011533067.1:c.1122T>C XP_011531369.1:p.Pro374=
NM_001363823.1:c.1119T>C NP_001350752.1:p.Pro373=
NM_001363875.1:c.1023T>C NP_001350804.1:p.Pro341=
XM_005264516.5:c.1119T>C XP_005264573.1:p.Pro373=
XM_011533067.2:c.1122T>C XP_011531369.1:p.Pro374=
XM_017004778.2:c.1026T>C XP_016860267.1:p.Pro342=
NM_001363823.2:c.1119T>C NP_001350752.1:p.Pro373=
NM_001363875.2:c.1023T>C NP_001350804.1:p.Pro341=
NM_001377959.1:c.1026T>C NP_001364888.1:p.Pro342=
NM_014946.4:c.1122T>C MANE Select NP_055761.2:p.Pro374=
NM_199436.2:c.1026T>C NP_955468.1:p.Pro342=