Canonical Allele Identifier: CA2500790303

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32128506_32128507del , CM000664.2:g.32128506_32128507del	GRCh38
NC_000002.11:g.32353575_32353576del , CM000664.1:g.32353575_32353576del	GRCh37
NC_000002.10:g.32207079_32207080del	NCBI36
NG_008730.1:g.69896_69897del , LRG_714:g.69896_69897del

Transcript Alleles

HGVS	Amino-acid change
ENST00000704289.1:c.*905+27_*905+28del	ENSP00000515816.1:n.*905+27_*905+28del
ENST00000315285.9:c.1245+27_1245+28del MANE Select	ENSP00000320885.3:n.1245+27_1245+28del
ENST00000621856.2:c.1242+27_1242+28del	ENSP00000482496.2:n.1242+27_1242+28del
ENST00000642281.1:c.983-8057_983-8056del
ENST00000642455.1:c.1146+27_1146+28del	ENSP00000493827.1:n.1146+27_1146+28del
ENST00000642751.1:c.1019+27_1019+28del
ENST00000642999.1:c.987+27_987+28del	ENSP00000496589.1:n.987+27_987+28del
ENST00000643327.1:c.404+27_404+28del
ENST00000643334.1:c.825+27_825+28del
ENST00000644408.1:c.1121+27_1121+28del
ENST00000644954.1:c.891+27_891+28del	ENSP00000494312.1:n.891+27_891+28del
ENST00000645159.1:n.1982+27_1982+28del
ENST00000645550.1:n.485_486del
ENST00000645671.1:c.695+27_695+28del
ENST00000645730.1:c.592+27_592+28del
ENST00000646082.1:c.891+27_891+28del
ENST00000646571.1:c.1149+27_1149+28del	ENSP00000495015.1:n.1149+27_1149+28del
ENST00000647007.1:n.937+27_937+28del
ENST00000647133.1:c.745+27_745+28del
ENST00000315285.7:c.1245+27_1245+28del	ENSP00000320885.3:n.1245+27_1245+28del
ENST00000345662.5:c.1149+27_1149+28del	ENSP00000340817.1:n.1149+27_1149+28del
ENST00000615843.4:c.1245+27_1245+28del	ENSP00000480893.1:n.1245+27_1245+28del
ENST00000621856.1:c.987+27_987+28del	ENSP00000482496.1:n.987+27_987+28del
NM_014946.3:c.1245+27_1245+28del , LRG_714t1:c.1245+27_1245+28del	NP_055761.2:n.1245+27_1245+28del
NM_199436.1:c.1149+27_1149+28del	NP_955468.1:n.1149+27_1149+28del
XM_005264516.3:c.1242+27_1242+28del	XP_005264573.1:n.1242+27_1242+28del
XM_011533067.1:c.1245+27_1245+28del	XP_011531369.1:n.1245+27_1245+28del
NM_001363823.1:c.1242+27_1242+28del	NP_001350752.1:n.1242+27_1242+28del
NM_001363875.1:c.1146+27_1146+28del	NP_001350804.1:n.1146+27_1146+28del
XM_005264516.5:c.1242+27_1242+28del	XP_005264573.1:n.1242+27_1242+28del
XM_011533067.2:c.1245+27_1245+28del	XP_011531369.1:n.1245+27_1245+28del
XM_017004778.2:c.1149+27_1149+28del	XP_016860267.1:n.1149+27_1149+28del
NM_001363823.2:c.1242+27_1242+28del	NP_001350752.1:n.1242+27_1242+28del
NM_001363875.2:c.1146+27_1146+28del	NP_001350804.1:n.1146+27_1146+28del
NM_001377959.1:c.1149+27_1149+28del	NP_001364888.1:n.1149+27_1149+28del
NM_014946.4:c.1245+27_1245+28del MANE Select	NP_055761.2:n.1245+27_1245+28del
NM_199436.2:c.1149+27_1149+28del	NP_955468.1:n.1149+27_1149+28del