Canonical Allele Identifier: CA2658522673

Gene: SPAST

Linked Data

• gnomAD v4: 2-32141835-CCTGTCATTTGCTGTTTCAGCTTTAAATTCAAAATTATATTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32141838_32141878del , CM000664.2:g.32141838_32141878del	GRCh38
NC_000002.11:g.32366907_32366947del , CM000664.1:g.32366907_32366947del	GRCh37
NC_000002.10:g.32220411_32220451del	NCBI36
NG_008730.1:g.83228_83268del , LRG_714:g.83228_83268del

Transcript Alleles

HGVS	Amino-acid change
ENST00000704289.1:c.*1154-66_*1154-26del	ENSP00000515816.1:n.*1154-66_*1154-26del
ENST00000315285.9:c.1494-66_1494-26del MANE Select	ENSP00000320885.3:n.1494-66_1494-26del
ENST00000621856.2:c.1491-66_1491-26del	ENSP00000482496.2:n.1491-66_1491-26del
ENST00000642281.1:c.1231-66_1231-26del
ENST00000642455.1:c.1395-66_1395-26del	ENSP00000493827.1:n.1395-66_1395-26del
ENST00000642751.1:c.1268-66_1268-26del
ENST00000642999.1:c.1236-66_1236-26del	ENSP00000496589.1:n.1236-66_1236-26del
ENST00000643327.1:c.561-66_561-26del
ENST00000643334.1:c.1074-66_1074-26del
ENST00000644408.1:c.1370-66_1370-26del
ENST00000644954.1:c.1140-66_1140-26del	ENSP00000494312.1:n.1140-66_1140-26del
ENST00000645159.1:n.2231-66_2231-26del
ENST00000645671.1:c.944-66_944-26del
ENST00000645730.1:c.673-66_673-26del
ENST00000646082.1:c.1140-66_1140-26del
ENST00000646571.1:c.1398-66_1398-26del	ENSP00000495015.1:n.1398-66_1398-26del
ENST00000647007.1:n.1186-66_1186-26del
ENST00000647133.1:c.994-66_994-26del
ENST00000315285.7:c.1494-66_1494-26del	ENSP00000320885.3:n.1494-66_1494-26del
ENST00000345662.5:c.1398-66_1398-26del	ENSP00000340817.1:n.1398-66_1398-26del
ENST00000615843.4:c.1494-66_1494-26del	ENSP00000480893.1:n.1494-66_1494-26del
ENST00000621856.1:c.1236-66_1236-26del	ENSP00000482496.1:n.1236-66_1236-26del
NM_014946.3:c.1494-66_1494-26del , LRG_714t1:c.1494-66_1494-26del	NP_055761.2:n.1494-66_1494-26del
NM_199436.1:c.1398-66_1398-26del	NP_955468.1:n.1398-66_1398-26del
XM_005264516.3:c.1491-66_1491-26del	XP_005264573.1:n.1491-66_1491-26del
XM_011533067.1:c.1494-66_1494-26del	XP_011531369.1:n.1494-66_1494-26del
NM_001363823.1:c.1491-66_1491-26del	NP_001350752.1:n.1491-66_1491-26del
NM_001363875.1:c.1395-66_1395-26del	NP_001350804.1:n.1395-66_1395-26del
XM_005264516.5:c.1491-66_1491-26del	XP_005264573.1:n.1491-66_1491-26del
XM_011533067.2:c.1494-66_1494-26del	XP_011531369.1:n.1494-66_1494-26del
XM_017004778.2:c.1398-66_1398-26del	XP_016860267.1:n.1398-66_1398-26del
NM_001363823.2:c.1491-66_1491-26del	NP_001350752.1:n.1491-66_1491-26del
NM_001363875.2:c.1395-66_1395-26del	NP_001350804.1:n.1395-66_1395-26del
NM_001377959.1:c.1398-66_1398-26del	NP_001364888.1:n.1398-66_1398-26del
NM_014946.4:c.1494-66_1494-26del MANE Select	NP_055761.2:n.1494-66_1494-26del
NM_199436.2:c.1398-66_1398-26del	NP_955468.1:n.1398-66_1398-26del