Canonical Allele Identifier: CA1242504438
Gene: SPAST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32141711_32141713delinsAAC , CM000664.2:g.32141711_32141713delinsAAC GRCh38
NC_000002.11:g.32366780_32366782delinsAAC , CM000664.1:g.32366780_32366782delinsAAC GRCh37
NC_000002.10:g.32220284_32220286delinsAAC NCBI36
NG_008730.1:g.83101_83103delinsAAC , LRG_714:g.83101_83103delinsAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000704289.1:c.*1154-193_*1154-191delinsAAC ENSP00000515816.1:n.*1154-193_*1154-191delinsAAC
ENST00000315285.9:c.1494-193_1494-191delinsAAC MANE Select ENSP00000320885.3:n.1494-193_1494-191delinsAAC
ENST00000621856.2:c.1491-193_1491-191delinsAAC ENSP00000482496.2:n.1491-193_1491-191delinsAAC
ENST00000642281.1:c.1231-193_1231-191delinsAAC
ENST00000642455.1:c.1395-193_1395-191delinsAAC ENSP00000493827.1:n.1395-193_1395-191delinsAAC
ENST00000642751.1:c.1268-193_1268-191delinsAAC
ENST00000642999.1:c.1236-193_1236-191delinsAAC ENSP00000496589.1:n.1236-193_1236-191delinsAAC
ENST00000643327.1:c.561-193_561-191delinsAAC
ENST00000643334.1:c.1074-193_1074-191delinsAAC
ENST00000644408.1:c.1370-193_1370-191delinsAAC
ENST00000644954.1:c.1140-193_1140-191delinsAAC ENSP00000494312.1:n.1140-193_1140-191delinsAAC
ENST00000645159.1:n.2231-193_2231-191delinsAAC
ENST00000645671.1:c.944-193_944-191delinsAAC
ENST00000645730.1:c.673-193_673-191delinsAAC
ENST00000646082.1:c.1140-193_1140-191delinsAAC
ENST00000646571.1:c.1398-193_1398-191delinsAAC ENSP00000495015.1:n.1398-193_1398-191delinsAAC
ENST00000647007.1:n.1186-193_1186-191delinsAAC
ENST00000647133.1:c.994-193_994-191delinsAAC
ENST00000315285.7:c.1494-193_1494-191delinsAAC ENSP00000320885.3:n.1494-193_1494-191delinsAAC
ENST00000345662.5:c.1398-193_1398-191delinsAAC ENSP00000340817.1:n.1398-193_1398-191delinsAAC
ENST00000615843.4:c.1494-193_1494-191delinsAAC ENSP00000480893.1:n.1494-193_1494-191delinsAAC
ENST00000621856.1:c.1236-193_1236-191delinsAAC ENSP00000482496.1:n.1236-193_1236-191delinsAAC
NM_014946.3:c.1494-193_1494-191delinsAAC , LRG_714t1:c.1494-193_1494-191delinsAAC NP_055761.2:n.1494-193_1494-191delinsAAC
NM_199436.1:c.1398-193_1398-191delinsAAC NP_955468.1:n.1398-193_1398-191delinsAAC
XM_005264516.3:c.1491-193_1491-191delinsAAC XP_005264573.1:n.1491-193_1491-191delinsAAC
XM_011533067.1:c.1494-193_1494-191delinsAAC XP_011531369.1:n.1494-193_1494-191delinsAAC
NM_001363823.1:c.1491-193_1491-191delinsAAC NP_001350752.1:n.1491-193_1491-191delinsAAC
NM_001363875.1:c.1395-193_1395-191delinsAAC NP_001350804.1:n.1395-193_1395-191delinsAAC
XM_005264516.5:c.1491-193_1491-191delinsAAC XP_005264573.1:n.1491-193_1491-191delinsAAC
XM_011533067.2:c.1494-193_1494-191delinsAAC XP_011531369.1:n.1494-193_1494-191delinsAAC
XM_017004778.2:c.1398-193_1398-191delinsAAC XP_016860267.1:n.1398-193_1398-191delinsAAC
NM_001363823.2:c.1491-193_1491-191delinsAAC NP_001350752.1:n.1491-193_1491-191delinsAAC
NM_001363875.2:c.1395-193_1395-191delinsAAC NP_001350804.1:n.1395-193_1395-191delinsAAC
NM_001377959.1:c.1398-193_1398-191delinsAAC NP_001364888.1:n.1398-193_1398-191delinsAAC
NM_014946.4:c.1494-193_1494-191delinsAAC MANE Select NP_055761.2:n.1494-193_1494-191delinsAAC
NM_199436.2:c.1398-193_1398-191delinsAAC NP_955468.1:n.1398-193_1398-191delinsAAC