Canonical Allele Identifier: CA1242504459

Gene: SPAST

Linked Data

• dbSNP Id: rs1679727519

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32141755_32141756del , CM000664.2:g.32141755_32141756del	GRCh38
NC_000002.11:g.32366824_32366825del , CM000664.1:g.32366824_32366825del	GRCh37
NC_000002.10:g.32220328_32220329del	NCBI36
NG_008730.1:g.83145_83146del , LRG_714:g.83145_83146del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*1154-149_*1154-148del	ENSP00000515816.1:n.*1154-149_*1154-148del
ENST00000315285.9:c.1494-149_1494-148del MANE Select	ENSP00000320885.3:n.1494-149_1494-148del
ENST00000621856.2:c.1491-149_1491-148del	ENSP00000482496.2:n.1491-149_1491-148del
ENST00000642281.1:c.1231-149_1231-148del
ENST00000642455.1:c.1395-149_1395-148del	ENSP00000493827.1:n.1395-149_1395-148del
ENST00000642751.1:c.1268-149_1268-148del
ENST00000642999.1:c.1236-149_1236-148del	ENSP00000496589.1:n.1236-149_1236-148del
ENST00000643327.1:c.561-149_561-148del
ENST00000643334.1:c.1074-149_1074-148del
ENST00000644408.1:c.1370-149_1370-148del
ENST00000644954.1:c.1140-149_1140-148del	ENSP00000494312.1:n.1140-149_1140-148del
ENST00000645159.1:n.2231-149_2231-148del
ENST00000645671.1:c.944-149_944-148del
ENST00000645730.1:c.673-149_673-148del
ENST00000646082.1:c.1140-149_1140-148del
ENST00000646571.1:c.1398-149_1398-148del	ENSP00000495015.1:n.1398-149_1398-148del
ENST00000647007.1:n.1186-149_1186-148del
ENST00000647133.1:c.994-149_994-148del
ENST00000315285.7:c.1494-149_1494-148del	ENSP00000320885.3:n.1494-149_1494-148del
ENST00000345662.5:c.1398-149_1398-148del	ENSP00000340817.1:n.1398-149_1398-148del
ENST00000615843.4:c.1494-149_1494-148del	ENSP00000480893.1:n.1494-149_1494-148del
ENST00000621856.1:c.1236-149_1236-148del	ENSP00000482496.1:n.1236-149_1236-148del
NM_014946.3:c.1494-149_1494-148del , LRG_714t1:c.1494-149_1494-148del	NP_055761.2:n.1494-149_1494-148del
NM_199436.1:c.1398-149_1398-148del	NP_955468.1:n.1398-149_1398-148del
XM_005264516.3:c.1491-149_1491-148del	XP_005264573.1:n.1491-149_1491-148del
XM_011533067.1:c.1494-149_1494-148del	XP_011531369.1:n.1494-149_1494-148del
NM_001363823.1:c.1491-149_1491-148del	NP_001350752.1:n.1491-149_1491-148del
NM_001363875.1:c.1395-149_1395-148del	NP_001350804.1:n.1395-149_1395-148del
XM_005264516.5:c.1491-149_1491-148del	XP_005264573.1:n.1491-149_1491-148del
XM_011533067.2:c.1494-149_1494-148del	XP_011531369.1:n.1494-149_1494-148del
XM_017004778.2:c.1398-149_1398-148del	XP_016860267.1:n.1398-149_1398-148del
NM_001363823.2:c.1491-149_1491-148del	NP_001350752.1:n.1491-149_1491-148del
NM_001363875.2:c.1395-149_1395-148del	NP_001350804.1:n.1395-149_1395-148del
NM_001377959.1:c.1398-149_1398-148del	NP_001364888.1:n.1398-149_1398-148del
NM_014946.4:c.1494-149_1494-148del MANE Select	NP_055761.2:n.1494-149_1494-148del
NM_199436.2:c.1398-149_1398-148del	NP_955468.1:n.1398-149_1398-148del