Canonical Allele Identifier: CA2658526519

Gene: SPAST

Linked Data

• gnomAD v4: 2-32126769-A-ACAC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32126769_32126770insCAC , CM000664.2:g.32126769_32126770insCAC	GRCh38
NC_000002.11:g.32351838_32351839insCAC , CM000664.1:g.32351838_32351839insCAC	GRCh37
NC_000002.10:g.32205342_32205343insCAC	NCBI36
NG_008730.1:g.68159_68160insCAC , LRG_714:g.68159_68160insCAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*759-179_*759-178insCAC	ENSP00000515816.1:n.*759-179_*759-178insCAC
ENST00000315285.9:c.1099-179_1099-178insCAC MANE Select	ENSP00000320885.3:n.1099-179_1099-178insCAC
ENST00000621856.2:c.1096-179_1096-178insCAC	ENSP00000482496.2:n.1096-179_1096-178insCAC
ENST00000642281.1:c.983-9794_983-9793insCAC
ENST00000642455.1:c.1000-179_1000-178insCAC	ENSP00000493827.1:n.1000-179_1000-178insCAC
ENST00000642751.1:c.873-179_873-178insCAC
ENST00000642999.1:c.841-179_841-178insCAC	ENSP00000496589.1:n.841-179_841-178insCAC
ENST00000643327.1:c.258-179_258-178insCAC
ENST00000643334.1:c.679-179_679-178insCAC
ENST00000644408.1:c.975-179_975-178insCAC
ENST00000644954.1:c.745-179_745-178insCAC	ENSP00000494312.1:n.745-179_745-178insCAC
ENST00000645159.1:n.272_273insCAC
ENST00000645550.1:n.133_134insCAC
ENST00000645671.1:c.549-179_549-178insCAC
ENST00000645730.1:c.446-179_446-178insCAC
ENST00000646082.1:c.745-179_745-178insCAC
ENST00000646571.1:c.1003-179_1003-178insCAC	ENSP00000495015.1:n.1003-179_1003-178insCAC
ENST00000647007.1:n.791-179_791-178insCAC
ENST00000647133.1:c.674-1639_674-1638insCAC
ENST00000315285.7:c.1099-179_1099-178insCAC	ENSP00000320885.3:n.1099-179_1099-178insCAC
ENST00000345662.5:c.1003-179_1003-178insCAC	ENSP00000340817.1:n.1003-179_1003-178insCAC
ENST00000615843.4:c.1099-179_1099-178insCAC	ENSP00000480893.1:n.1099-179_1099-178insCAC
ENST00000621856.1:c.841-179_841-178insCAC	ENSP00000482496.1:n.841-179_841-178insCAC
NM_014946.3:c.1099-179_1099-178insCAC , LRG_714t1:c.1099-179_1099-178insCAC	NP_055761.2:n.1099-179_1099-178insCAC
NM_199436.1:c.1003-179_1003-178insCAC	NP_955468.1:n.1003-179_1003-178insCAC
XM_005264516.3:c.1096-179_1096-178insCAC	XP_005264573.1:n.1096-179_1096-178insCAC
XM_011533067.1:c.1099-179_1099-178insCAC	XP_011531369.1:n.1099-179_1099-178insCAC
NM_001363823.1:c.1096-179_1096-178insCAC	NP_001350752.1:n.1096-179_1096-178insCAC
NM_001363875.1:c.1000-179_1000-178insCAC	NP_001350804.1:n.1000-179_1000-178insCAC
XM_005264516.5:c.1096-179_1096-178insCAC	XP_005264573.1:n.1096-179_1096-178insCAC
XM_011533067.2:c.1099-179_1099-178insCAC	XP_011531369.1:n.1099-179_1099-178insCAC
XM_017004778.2:c.1003-179_1003-178insCAC	XP_016860267.1:n.1003-179_1003-178insCAC
NM_001363823.2:c.1096-179_1096-178insCAC	NP_001350752.1:n.1096-179_1096-178insCAC
NM_001363875.2:c.1000-179_1000-178insCAC	NP_001350804.1:n.1000-179_1000-178insCAC
NM_001377959.1:c.1003-179_1003-178insCAC	NP_001364888.1:n.1003-179_1003-178insCAC
NM_014946.4:c.1099-179_1099-178insCAC MANE Select	NP_055761.2:n.1099-179_1099-178insCAC
NM_199436.2:c.1003-179_1003-178insCAC	NP_955468.1:n.1003-179_1003-178insCAC