Canonical Allele Identifier: CA1242501022

Gene: SPAST

Linked Data

• dbSNP Id: rs1679541530

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32136543_32136544insATC , CM000664.2:g.32136543_32136544insATC	GRCh38
NC_000002.11:g.32361612_32361613insATC , CM000664.1:g.32361612_32361613insATC	GRCh37
NC_000002.10:g.32215116_32215117insATC	NCBI36
NG_008730.1:g.77933_77934insATC , LRG_714:g.77933_77934insATC

Transcript Alleles

HGVS	Amino-acid change
ENST00000704289.1:c.*906-20_*906-19insATC	ENSP00000515816.1:n.*906-20_*906-19insATC...
ENST00000315285.9:c.1246-20_1246-19insATC MANE Select	ENSP00000320885.3:n.1246-20_1246-19insATC...
ENST00000621856.2:c.1243-20_1243-19insATC	ENSP00000482496.2:n.1243-20_1243-19insATC...
ENST00000642281.1:c.983-20_983-19insATC
ENST00000642455.1:c.1147-20_1147-19insATC	ENSP00000493827.1:n.1147-20_1147-19insATC...
ENST00000642751.1:c.1020-20_1020-19insATC
ENST00000642999.1:c.988-20_988-19insATC	ENSP00000496589.1:n.988-20_988-19insATC
ENST00000643327.1:c.405-20_405-19insATC
ENST00000643334.1:c.826-20_826-19insATC
ENST00000644408.1:c.1122-20_1122-19insATC
ENST00000644954.1:c.892-20_892-19insATC	ENSP00000494312.1:n.892-20_892-19insATC
ENST00000645159.1:n.1983-20_1983-19insATC
ENST00000645671.1:c.696-20_696-19insATC
ENST00000645730.1:c.593-566_593-565insATC
ENST00000646082.1:c.892-20_892-19insATC
ENST00000646571.1:c.1150-20_1150-19insATC	ENSP00000495015.1:n.1150-20_1150-19insATC...
ENST00000647007.1:n.938-20_938-19insATC
ENST00000647133.1:c.746-20_746-19insATC
ENST00000315285.7:c.1246-20_1246-19insATC	ENSP00000320885.3:n.1246-20_1246-19insATC...
ENST00000345662.5:c.1150-20_1150-19insATC	ENSP00000340817.1:n.1150-20_1150-19insATC...
ENST00000615843.4:c.1246-20_1246-19insATC	ENSP00000480893.1:n.1246-20_1246-19insATC...
ENST00000621856.1:c.988-20_988-19insATC	ENSP00000482496.1:n.988-20_988-19insATC
NM_014946.3:c.1246-20_1246-19insATC , LRG_714t1:c.1246-20_1246-19insATC	NP_055761.2:n.1246-20_1246-19insATC
NM_199436.1:c.1150-20_1150-19insATC	NP_955468.1:n.1150-20_1150-19insATC
XM_005264516.3:c.1243-20_1243-19insATC	XP_005264573.1:n.1243-20_1243-19insATC
XM_011533067.1:c.1246-20_1246-19insATC	XP_011531369.1:n.1246-20_1246-19insATC
NM_001363823.1:c.1243-20_1243-19insATC	NP_001350752.1:n.1243-20_1243-19insATC
NM_001363875.1:c.1147-20_1147-19insATC	NP_001350804.1:n.1147-20_1147-19insATC
XM_005264516.5:c.1243-20_1243-19insATC	XP_005264573.1:n.1243-20_1243-19insATC
XM_011533067.2:c.1246-20_1246-19insATC	XP_011531369.1:n.1246-20_1246-19insATC
XM_017004778.2:c.1150-20_1150-19insATC	XP_016860267.1:n.1150-20_1150-19insATC
NM_001363823.2:c.1243-20_1243-19insATC	NP_001350752.1:n.1243-20_1243-19insATC
NM_001363875.2:c.1147-20_1147-19insATC	NP_001350804.1:n.1147-20_1147-19insATC
NM_001377959.1:c.1150-20_1150-19insATC	NP_001364888.1:n.1150-20_1150-19insATC
NM_014946.4:c.1246-20_1246-19insATC MANE Select	NP_055761.2:n.1246-20_1246-19insATC
NM_199436.2:c.1150-20_1150-19insATC	NP_955468.1:n.1150-20_1150-19insATC