Canonical Allele Identifier: CA2658526622
Gene: SPAST HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32126940_32126941insA , CM000664.2:g.32126940_32126941insA GRCh38
NC_000002.11:g.32352009_32352010insA , CM000664.1:g.32352009_32352010insA GRCh37
NC_000002.10:g.32205513_32205514insA NCBI36
NG_008730.1:g.68330_68331insA , LRG_714:g.68330_68331insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.*759-8_*759-7insA ENSP00000515816.1:n.*759-8_*759-7insA
ENST00000315285.9:c.1099-8_1099-7insA MANE Select ENSP00000320885.3:n.1099-8_1099-7insA
ENST00000621856.2:c.1096-8_1096-7insA ENSP00000482496.2:n.1096-8_1096-7insA
ENST00000642281.1:c.983-9623_983-9622insA
ENST00000642455.1:c.1000-8_1000-7insA ENSP00000493827.1:n.1000-8_1000-7insA
ENST00000642751.1:c.873-8_873-7insA
ENST00000642999.1:c.841-8_841-7insA ENSP00000496589.1:n.841-8_841-7insA
ENST00000643327.1:c.258-8_258-7insA
ENST00000643334.1:c.679-8_679-7insA
ENST00000644408.1:c.975-8_975-7insA
ENST00000644954.1:c.745-8_745-7insA ENSP00000494312.1:n.745-8_745-7insA
ENST00000645159.1:n.443_444insA
ENST00000645550.1:n.304_305insA
ENST00000645671.1:c.549-8_549-7insA
ENST00000645730.1:c.446-8_446-7insA
ENST00000646082.1:c.745-8_745-7insA
ENST00000646571.1:c.1003-8_1003-7insA ENSP00000495015.1:n.1003-8_1003-7insA
ENST00000647007.1:n.791-8_791-7insA
ENST00000647133.1:c.674-1468_674-1467insA
ENST00000315285.7:c.1099-8_1099-7insA ENSP00000320885.3:n.1099-8_1099-7insA
ENST00000345662.5:c.1003-8_1003-7insA ENSP00000340817.1:n.1003-8_1003-7insA
ENST00000615843.4:c.1099-8_1099-7insA ENSP00000480893.1:n.1099-8_1099-7insA
ENST00000621856.1:c.841-8_841-7insA ENSP00000482496.1:n.841-8_841-7insA
NM_014946.3:c.1099-8_1099-7insA , LRG_714t1:c.1099-8_1099-7insA NP_055761.2:n.1099-8_1099-7insA
NM_199436.1:c.1003-8_1003-7insA NP_955468.1:n.1003-8_1003-7insA
XM_005264516.3:c.1096-8_1096-7insA XP_005264573.1:n.1096-8_1096-7insA
XM_011533067.1:c.1099-8_1099-7insA XP_011531369.1:n.1099-8_1099-7insA
NM_001363823.1:c.1096-8_1096-7insA NP_001350752.1:n.1096-8_1096-7insA
NM_001363875.1:c.1000-8_1000-7insA NP_001350804.1:n.1000-8_1000-7insA
XM_005264516.5:c.1096-8_1096-7insA XP_005264573.1:n.1096-8_1096-7insA
XM_011533067.2:c.1099-8_1099-7insA XP_011531369.1:n.1099-8_1099-7insA
XM_017004778.2:c.1003-8_1003-7insA XP_016860267.1:n.1003-8_1003-7insA
NM_001363823.2:c.1096-8_1096-7insA NP_001350752.1:n.1096-8_1096-7insA
NM_001363875.2:c.1000-8_1000-7insA NP_001350804.1:n.1000-8_1000-7insA
NM_001377959.1:c.1003-8_1003-7insA NP_001364888.1:n.1003-8_1003-7insA
NM_014946.4:c.1099-8_1099-7insA MANE Select NP_055761.2:n.1099-8_1099-7insA
NM_199436.2:c.1003-8_1003-7insA NP_955468.1:n.1003-8_1003-7insA