Canonical Allele Identifier: CA1242497485

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32127135G= , CM000664.2:g.32127135G=	GRCh38
NC_000002.11:g.32352204G= , CM000664.1:g.32352204G=	GRCh37
NC_000002.10:g.32205708G=	NCBI36
NG_008730.1:g.68525G= , LRG_714:g.68525G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*833+113G=	ENSP00000515816.1:n.*833+113G=
ENST00000315285.9:c.1173+113G= MANE Select	ENSP00000320885.3:n.1173+113G=
ENST00000621856.2:c.1170+113G=	ENSP00000482496.2:n.1170+113G=
ENST00000642281.1:c.983-9428G=
ENST00000642455.1:c.1074+113G=	ENSP00000493827.1:n.1074+113G=
ENST00000642751.1:c.947+113G=
ENST00000642999.1:c.915+113G=	ENSP00000496589.1:n.915+113G=
ENST00000643327.1:c.332+113G=
ENST00000643334.1:c.753+113G=
ENST00000644408.1:c.1049+113G=
ENST00000644954.1:c.819+113G=	ENSP00000494312.1:n.819+113G=
ENST00000645159.1:n.638G=
ENST00000645550.1:n.386+113G=
ENST00000645671.1:c.623+113G=
ENST00000645730.1:c.520+113G=
ENST00000646082.1:c.819+113G=
ENST00000646571.1:c.1077+113G=	ENSP00000495015.1:n.1077+113G=
ENST00000647007.1:n.865+113G=
ENST00000647133.1:c.674-1273G=
ENST00000315285.7:c.1173+113G=	ENSP00000320885.3:n.1173+113G=
ENST00000345662.5:c.1077+113G=	ENSP00000340817.1:n.1077+113G=
ENST00000615843.4:c.1173+113G=	ENSP00000480893.1:n.1173+113G=
ENST00000621856.1:c.915+113G=	ENSP00000482496.1:n.915+113G=
NM_014946.3:c.1173+113G= , LRG_714t1:c.1173+113G=	NP_055761.2:n.1173+113G=
NM_199436.1:c.1077+113G=	NP_955468.1:n.1077+113G=
XM_005264516.3:c.1170+113G=	XP_005264573.1:n.1170+113G=
XM_011533067.1:c.1173+113G=	XP_011531369.1:n.1173+113G=
NM_001363823.1:c.1170+113G=	NP_001350752.1:n.1170+113G=
NM_001363875.1:c.1074+113G=	NP_001350804.1:n.1074+113G=
XM_005264516.5:c.1170+113G=	XP_005264573.1:n.1170+113G=
XM_011533067.2:c.1173+113G=	XP_011531369.1:n.1173+113G=
XM_017004778.2:c.1077+113G=	XP_016860267.1:n.1077+113G=
NM_001363823.2:c.1170+113G=	NP_001350752.1:n.1170+113G=
NM_001363875.2:c.1074+113G=	NP_001350804.1:n.1074+113G=
NM_001377959.1:c.1077+113G=	NP_001364888.1:n.1077+113G=
NM_014946.4:c.1173+113G= MANE Select	NP_055761.2:n.1173+113G=
NM_199436.2:c.1077+113G=	NP_955468.1:n.1077+113G=