Canonical Allele Identifier: CA1242500887

Gene: SPAST

Linked Data

• dbSNP Id: rs1679536775

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32136382_32136383del , CM000664.2:g.32136382_32136383del	GRCh38
NC_000002.11:g.32361451_32361452del , CM000664.1:g.32361451_32361452del	GRCh37
NC_000002.10:g.32214955_32214956del	NCBI36
NG_008730.1:g.77772_77773del , LRG_714:g.77772_77773del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*906-181_*906-180del	ENSP00000515816.1:n.*906-181_*906-180del
ENST00000315285.9:c.1246-181_1246-180del MANE Select	ENSP00000320885.3:n.1246-181_1246-180del
ENST00000621856.2:c.1243-181_1243-180del	ENSP00000482496.2:n.1243-181_1243-180del
ENST00000642281.1:c.983-181_983-180del
ENST00000642455.1:c.1147-181_1147-180del	ENSP00000493827.1:n.1147-181_1147-180del
ENST00000642751.1:c.1020-181_1020-180del
ENST00000642999.1:c.988-181_988-180del	ENSP00000496589.1:n.988-181_988-180del
ENST00000643327.1:c.405-181_405-180del
ENST00000643334.1:c.826-181_826-180del
ENST00000644408.1:c.1122-181_1122-180del
ENST00000644954.1:c.892-181_892-180del	ENSP00000494312.1:n.892-181_892-180del
ENST00000645159.1:n.1983-181_1983-180del
ENST00000645671.1:c.696-181_696-180del
ENST00000645730.1:c.593-727_593-726del
ENST00000646082.1:c.892-181_892-180del
ENST00000646571.1:c.1150-181_1150-180del	ENSP00000495015.1:n.1150-181_1150-180del
ENST00000647007.1:n.938-181_938-180del
ENST00000647133.1:c.746-181_746-180del
ENST00000315285.7:c.1246-181_1246-180del	ENSP00000320885.3:n.1246-181_1246-180del
ENST00000345662.5:c.1150-181_1150-180del	ENSP00000340817.1:n.1150-181_1150-180del
ENST00000615843.4:c.1246-181_1246-180del	ENSP00000480893.1:n.1246-181_1246-180del
ENST00000621856.1:c.988-181_988-180del	ENSP00000482496.1:n.988-181_988-180del
NM_014946.3:c.1246-181_1246-180del , LRG_714t1:c.1246-181_1246-180del	NP_055761.2:n.1246-181_1246-180del
NM_199436.1:c.1150-181_1150-180del	NP_955468.1:n.1150-181_1150-180del
XM_005264516.3:c.1243-181_1243-180del	XP_005264573.1:n.1243-181_1243-180del
XM_011533067.1:c.1246-181_1246-180del	XP_011531369.1:n.1246-181_1246-180del
NM_001363823.1:c.1243-181_1243-180del	NP_001350752.1:n.1243-181_1243-180del
NM_001363875.1:c.1147-181_1147-180del	NP_001350804.1:n.1147-181_1147-180del
XM_005264516.5:c.1243-181_1243-180del	XP_005264573.1:n.1243-181_1243-180del
XM_011533067.2:c.1246-181_1246-180del	XP_011531369.1:n.1246-181_1246-180del
XM_017004778.2:c.1150-181_1150-180del	XP_016860267.1:n.1150-181_1150-180del
NM_001363823.2:c.1243-181_1243-180del	NP_001350752.1:n.1243-181_1243-180del
NM_001363875.2:c.1147-181_1147-180del	NP_001350804.1:n.1147-181_1147-180del
NM_001377959.1:c.1150-181_1150-180del	NP_001364888.1:n.1150-181_1150-180del
NM_014946.4:c.1246-181_1246-180del MANE Select	NP_055761.2:n.1246-181_1246-180del
NM_199436.2:c.1150-181_1150-180del	NP_955468.1:n.1150-181_1150-180del