Canonical Allele Identifier: CA1242497394

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32126954A= , CM000664.2:g.32126954A=	GRCh38
NC_000002.11:g.32352023A= , CM000664.1:g.32352023A=	GRCh37
NC_000002.10:g.32205527A=	NCBI36
NG_008730.1:g.68344A= , LRG_714:g.68344A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*765A=	ENSP00000515816.1:n.*765A=
ENST00000315285.9:c.1105A= MANE Select	ENSP00000320885.3:p.Thr369=
ENST00000621856.2:c.1102A=	ENSP00000482496.2:p.Thr368=
ENST00000642281.1:c.983-9609A=
ENST00000642455.1:c.1006A=	ENSP00000493827.1:p.Thr336=
ENST00000642751.1:c.879A=
ENST00000642999.1:c.847A=	ENSP00000496589.1:p.Thr283=
ENST00000643327.1:c.264A=
ENST00000643334.1:c.685A=
ENST00000644408.1:c.981A=
ENST00000644954.1:c.751A=	ENSP00000494312.1:p.Thr251=
ENST00000645159.1:n.457A=
ENST00000645550.1:n.318A=
ENST00000645671.1:c.555A=
ENST00000645730.1:c.452A=
ENST00000646082.1:c.751A=
ENST00000646571.1:c.1009A=	ENSP00000495015.1:p.Thr337=
ENST00000647007.1:n.797A=
ENST00000647133.1:c.674-1454A=
ENST00000315285.7:c.1105A=	ENSP00000320885.3:p.Thr369=
ENST00000345662.5:c.1009A=	ENSP00000340817.1:p.Thr337=
ENST00000615843.4:c.1105A=	ENSP00000480893.1:p.Thr369=
ENST00000621856.1:c.847A=	ENSP00000482496.1:p.Thr283=
NM_014946.3:c.1105A= , LRG_714t1:c.1105A=	NP_055761.2:p.Thr369=
NM_199436.1:c.1009A=	NP_955468.1:p.Thr337=
XM_005264516.3:c.1102A=	XP_005264573.1:p.Thr368=
XM_011533067.1:c.1105A=	XP_011531369.1:p.Thr369=
NM_001363823.1:c.1102A=	NP_001350752.1:p.Thr368=
NM_001363875.1:c.1006A=	NP_001350804.1:p.Thr336=
XM_005264516.5:c.1102A=	XP_005264573.1:p.Thr368=
XM_011533067.2:c.1105A=	XP_011531369.1:p.Thr369=
XM_017004778.2:c.1009A=	XP_016860267.1:p.Thr337=
NM_001363823.2:c.1102A=	NP_001350752.1:p.Thr368=
NM_001363875.2:c.1006A=	NP_001350804.1:p.Thr336=
NM_001377959.1:c.1009A=	NP_001364888.1:p.Thr337=
NM_014946.4:c.1105A= MANE Select	NP_055761.2:p.Thr369=
NM_199436.2:c.1009A=	NP_955468.1:p.Thr337=