Canonical Allele Identifier: CA425448374

Gene: SPAST

Linked Data

• MyVariant Identifiers: chr2:g.32361656A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32136587A>C , CM000664.2:g.32136587A>C	GRCh38
NC_000002.11:g.32361656A>C , CM000664.1:g.32361656A>C	GRCh37
NC_000002.10:g.32215160A>C	NCBI36
NG_008730.1:g.77977A>C , LRG_714:g.77977A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*930A>C	ENSP00000515816.1:n.*930A>C
ENST00000315285.9:c.1270A>C MANE Select	ENSP00000320885.3:p.Arg424=
ENST00000621856.2:c.1267A>C	ENSP00000482496.2:p.Arg423=
ENST00000642281.1:c.1007A>C
ENST00000642455.1:c.1171A>C	ENSP00000493827.1:p.Arg391=
ENST00000642751.1:c.1044A>C
ENST00000642999.1:c.1012A>C	ENSP00000496589.1:p.Arg338=
ENST00000643327.1:c.429A>C
ENST00000643334.1:c.850A>C
ENST00000644408.1:c.1146A>C
ENST00000644954.1:c.916A>C	ENSP00000494312.1:p.Arg306=
ENST00000645159.1:n.2007A>C
ENST00000645671.1:c.720A>C
ENST00000645730.1:c.593-522A>C
ENST00000646082.1:c.916A>C
ENST00000646571.1:c.1174A>C	ENSP00000495015.1:p.Arg392=
ENST00000647007.1:n.962A>C
ENST00000647133.1:c.770A>C
ENST00000315285.7:c.1270A>C	ENSP00000320885.3:p.Arg424=
ENST00000345662.5:c.1174A>C	ENSP00000340817.1:p.Arg392=
ENST00000615843.4:c.1270A>C	ENSP00000480893.1:p.Arg424=
ENST00000621856.1:c.1012A>C	ENSP00000482496.1:p.Arg338=
NM_014946.3:c.1270A>C , LRG_714t1:c.1270A>C	NP_055761.2:p.Arg424=
NM_199436.1:c.1174A>C	NP_955468.1:p.Arg392=
XM_005264516.3:c.1267A>C	XP_005264573.1:p.Arg423=
XM_011533067.1:c.1270A>C	XP_011531369.1:p.Arg424=
NM_001363823.1:c.1267A>C	NP_001350752.1:p.Arg423=
NM_001363875.1:c.1171A>C	NP_001350804.1:p.Arg391=
XM_005264516.5:c.1267A>C	XP_005264573.1:p.Arg423=
XM_011533067.2:c.1270A>C	XP_011531369.1:p.Arg424=
XM_017004778.2:c.1174A>C	XP_016860267.1:p.Arg392=
NM_001363823.2:c.1267A>C	NP_001350752.1:p.Arg423=
NM_001363875.2:c.1171A>C	NP_001350804.1:p.Arg391=
NM_001377959.1:c.1174A>C	NP_001364888.1:p.Arg392=
NM_014946.4:c.1270A>C MANE Select	NP_055761.2:p.Arg424=
NM_199436.2:c.1174A>C	NP_955468.1:p.Arg392=