Canonical Allele Identifier: CA2658522667
Gene: SPAST HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32141817_32141818insTTT , CM000664.2:g.32141817_32141818insTTT GRCh38
NC_000002.11:g.32366886_32366887insTTT , CM000664.1:g.32366886_32366887insTTT GRCh37
NC_000002.10:g.32220390_32220391insTTT NCBI36
NG_008730.1:g.83207_83208insTTT , LRG_714:g.83207_83208insTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000704289.1:c.*1154-87_*1154-86insTTT ENSP00000515816.1:n.*1154-87_*1154-86insT...
ENST00000315285.9:c.1494-87_1494-86insTTT MANE Select ENSP00000320885.3:n.1494-87_1494-86insTTT...
ENST00000621856.2:c.1491-87_1491-86insTTT ENSP00000482496.2:n.1491-87_1491-86insTTT...
ENST00000642281.1:c.1231-87_1231-86insTTT
ENST00000642455.1:c.1395-87_1395-86insTTT ENSP00000493827.1:n.1395-87_1395-86insTTT...
ENST00000642751.1:c.1268-87_1268-86insTTT
ENST00000642999.1:c.1236-87_1236-86insTTT ENSP00000496589.1:n.1236-87_1236-86insTTT...
ENST00000643327.1:c.561-87_561-86insTTT
ENST00000643334.1:c.1074-87_1074-86insTTT
ENST00000644408.1:c.1370-87_1370-86insTTT
ENST00000644954.1:c.1140-87_1140-86insTTT ENSP00000494312.1:n.1140-87_1140-86insTTT...
ENST00000645159.1:n.2231-87_2231-86insTTT
ENST00000645671.1:c.944-87_944-86insTTT
ENST00000645730.1:c.673-87_673-86insTTT
ENST00000646082.1:c.1140-87_1140-86insTTT
ENST00000646571.1:c.1398-87_1398-86insTTT ENSP00000495015.1:n.1398-87_1398-86insTTT...
ENST00000647007.1:n.1186-87_1186-86insTTT
ENST00000647133.1:c.994-87_994-86insTTT
ENST00000315285.7:c.1494-87_1494-86insTTT ENSP00000320885.3:n.1494-87_1494-86insTTT...
ENST00000345662.5:c.1398-87_1398-86insTTT ENSP00000340817.1:n.1398-87_1398-86insTTT...
ENST00000615843.4:c.1494-87_1494-86insTTT ENSP00000480893.1:n.1494-87_1494-86insTTT...
ENST00000621856.1:c.1236-87_1236-86insTTT ENSP00000482496.1:n.1236-87_1236-86insTTT...
NM_014946.3:c.1494-87_1494-86insTTT , LRG_714t1:c.1494-87_1494-86insTTT NP_055761.2:n.1494-87_1494-86insTTT
NM_199436.1:c.1398-87_1398-86insTTT NP_955468.1:n.1398-87_1398-86insTTT
XM_005264516.3:c.1491-87_1491-86insTTT XP_005264573.1:n.1491-87_1491-86insTTT
XM_011533067.1:c.1494-87_1494-86insTTT XP_011531369.1:n.1494-87_1494-86insTTT
NM_001363823.1:c.1491-87_1491-86insTTT NP_001350752.1:n.1491-87_1491-86insTTT
NM_001363875.1:c.1395-87_1395-86insTTT NP_001350804.1:n.1395-87_1395-86insTTT
XM_005264516.5:c.1491-87_1491-86insTTT XP_005264573.1:n.1491-87_1491-86insTTT
XM_011533067.2:c.1494-87_1494-86insTTT XP_011531369.1:n.1494-87_1494-86insTTT
XM_017004778.2:c.1398-87_1398-86insTTT XP_016860267.1:n.1398-87_1398-86insTTT
NM_001363823.2:c.1491-87_1491-86insTTT NP_001350752.1:n.1491-87_1491-86insTTT
NM_001363875.2:c.1395-87_1395-86insTTT NP_001350804.1:n.1395-87_1395-86insTTT
NM_001377959.1:c.1398-87_1398-86insTTT NP_001364888.1:n.1398-87_1398-86insTTT
NM_014946.4:c.1494-87_1494-86insTTT MANE Select NP_055761.2:n.1494-87_1494-86insTTT
NM_199436.2:c.1398-87_1398-86insTTT NP_955468.1:n.1398-87_1398-86insTTT