Canonical Allele Identifier: CA767795736

Gene: SPAST

Linked Data

• dbSNP Id: rs1387671521
• MyVariant Identifiers: chr2:g.32366803_32366810del (hg19) ; chr2:g.32141734_32141741del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32141735_32141742del , CM000664.2:g.32141735_32141742del	GRCh38
NC_000002.11:g.32366804_32366811del , CM000664.1:g.32366804_32366811del	GRCh37
NC_000002.10:g.32220308_32220315del	NCBI36
NG_008730.1:g.83125_83132del , LRG_714:g.83125_83132del

Transcript Alleles

HGVS	Amino-acid change
ENST00000704289.1:c.*1154-169_*1154-162del	ENSP00000515816.1:n.*1154-169_*1154-162del
ENST00000315285.9:c.1494-169_1494-162del MANE Select	ENSP00000320885.3:n.1494-169_1494-162del
ENST00000621856.2:c.1491-169_1491-162del	ENSP00000482496.2:n.1491-169_1491-162del
ENST00000642281.1:c.1231-169_1231-162del
ENST00000642455.1:c.1395-169_1395-162del	ENSP00000493827.1:n.1395-169_1395-162del
ENST00000642751.1:c.1268-169_1268-162del
ENST00000642999.1:c.1236-169_1236-162del	ENSP00000496589.1:n.1236-169_1236-162del
ENST00000643327.1:c.561-169_561-162del
ENST00000643334.1:c.1074-169_1074-162del
ENST00000644408.1:c.1370-169_1370-162del
ENST00000644954.1:c.1140-169_1140-162del	ENSP00000494312.1:n.1140-169_1140-162del
ENST00000645159.1:n.2231-169_2231-162del
ENST00000645671.1:c.944-169_944-162del
ENST00000645730.1:c.673-169_673-162del
ENST00000646082.1:c.1140-169_1140-162del
ENST00000646571.1:c.1398-169_1398-162del	ENSP00000495015.1:n.1398-169_1398-162del
ENST00000647007.1:n.1186-169_1186-162del
ENST00000647133.1:c.994-169_994-162del
ENST00000315285.7:c.1494-169_1494-162del	ENSP00000320885.3:n.1494-169_1494-162del
ENST00000345662.5:c.1398-169_1398-162del	ENSP00000340817.1:n.1398-169_1398-162del
ENST00000615843.4:c.1494-169_1494-162del	ENSP00000480893.1:n.1494-169_1494-162del
ENST00000621856.1:c.1236-169_1236-162del	ENSP00000482496.1:n.1236-169_1236-162del
NM_014946.3:c.1494-169_1494-162del , LRG_714t1:c.1494-169_1494-162del	NP_055761.2:n.1494-169_1494-162del
NM_199436.1:c.1398-169_1398-162del	NP_955468.1:n.1398-169_1398-162del
XM_005264516.3:c.1491-169_1491-162del	XP_005264573.1:n.1491-169_1491-162del
XM_011533067.1:c.1494-169_1494-162del	XP_011531369.1:n.1494-169_1494-162del
NM_001363823.1:c.1491-169_1491-162del	NP_001350752.1:n.1491-169_1491-162del
NM_001363875.1:c.1395-169_1395-162del	NP_001350804.1:n.1395-169_1395-162del
XM_005264516.5:c.1491-169_1491-162del	XP_005264573.1:n.1491-169_1491-162del
XM_011533067.2:c.1494-169_1494-162del	XP_011531369.1:n.1494-169_1494-162del
XM_017004778.2:c.1398-169_1398-162del	XP_016860267.1:n.1398-169_1398-162del
NM_001363823.2:c.1491-169_1491-162del	NP_001350752.1:n.1491-169_1491-162del
NM_001363875.2:c.1395-169_1395-162del	NP_001350804.1:n.1395-169_1395-162del
NM_001377959.1:c.1398-169_1398-162del	NP_001364888.1:n.1398-169_1398-162del
NM_014946.4:c.1494-169_1494-162del MANE Select	NP_055761.2:n.1494-169_1494-162del
NM_199436.2:c.1398-169_1398-162del	NP_955468.1:n.1398-169_1398-162del