Canonical Allele Identifier: CA2658526515

Gene: SPAST

Linked Data

• gnomAD v4: 2-32126764-GTGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32126765_32126767del , CM000664.2:g.32126765_32126767del	GRCh38
NC_000002.11:g.32351834_32351836del , CM000664.1:g.32351834_32351836del	GRCh37
NC_000002.10:g.32205338_32205340del	NCBI36
NG_008730.1:g.68155_68157del , LRG_714:g.68155_68157del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*759-183_*759-181del	ENSP00000515816.1:n.*759-183_*759-181del
ENST00000315285.9:c.1099-183_1099-181del MANE Select	ENSP00000320885.3:n.1099-183_1099-181del
ENST00000621856.2:c.1096-183_1096-181del	ENSP00000482496.2:n.1096-183_1096-181del
ENST00000642281.1:c.983-9798_983-9796del
ENST00000642455.1:c.1000-183_1000-181del	ENSP00000493827.1:n.1000-183_1000-181del
ENST00000642751.1:c.873-183_873-181del
ENST00000642999.1:c.841-183_841-181del	ENSP00000496589.1:n.841-183_841-181del
ENST00000643327.1:c.258-183_258-181del
ENST00000643334.1:c.679-183_679-181del
ENST00000644408.1:c.975-183_975-181del
ENST00000644954.1:c.745-183_745-181del	ENSP00000494312.1:n.745-183_745-181del
ENST00000645159.1:n.268_270del
ENST00000645550.1:n.129_131del
ENST00000645671.1:c.549-183_549-181del
ENST00000645730.1:c.446-183_446-181del
ENST00000646082.1:c.745-183_745-181del
ENST00000646571.1:c.1003-183_1003-181del	ENSP00000495015.1:n.1003-183_1003-181del
ENST00000647007.1:n.791-183_791-181del
ENST00000647133.1:c.674-1643_674-1641del
ENST00000315285.7:c.1099-183_1099-181del	ENSP00000320885.3:n.1099-183_1099-181del
ENST00000345662.5:c.1003-183_1003-181del	ENSP00000340817.1:n.1003-183_1003-181del
ENST00000615843.4:c.1099-183_1099-181del	ENSP00000480893.1:n.1099-183_1099-181del
ENST00000621856.1:c.841-183_841-181del	ENSP00000482496.1:n.841-183_841-181del
NM_014946.3:c.1099-183_1099-181del , LRG_714t1:c.1099-183_1099-181del	NP_055761.2:n.1099-183_1099-181del
NM_199436.1:c.1003-183_1003-181del	NP_955468.1:n.1003-183_1003-181del
XM_005264516.3:c.1096-183_1096-181del	XP_005264573.1:n.1096-183_1096-181del
XM_011533067.1:c.1099-183_1099-181del	XP_011531369.1:n.1099-183_1099-181del
NM_001363823.1:c.1096-183_1096-181del	NP_001350752.1:n.1096-183_1096-181del
NM_001363875.1:c.1000-183_1000-181del	NP_001350804.1:n.1000-183_1000-181del
XM_005264516.5:c.1096-183_1096-181del	XP_005264573.1:n.1096-183_1096-181del
XM_011533067.2:c.1099-183_1099-181del	XP_011531369.1:n.1099-183_1099-181del
XM_017004778.2:c.1003-183_1003-181del	XP_016860267.1:n.1003-183_1003-181del
NM_001363823.2:c.1096-183_1096-181del	NP_001350752.1:n.1096-183_1096-181del
NM_001363875.2:c.1000-183_1000-181del	NP_001350804.1:n.1000-183_1000-181del
NM_001377959.1:c.1003-183_1003-181del	NP_001364888.1:n.1003-183_1003-181del
NM_014946.4:c.1099-183_1099-181del MANE Select	NP_055761.2:n.1099-183_1099-181del
NM_199436.2:c.1003-183_1003-181del	NP_955468.1:n.1003-183_1003-181del