Canonical Allele Identifier: CA346505541

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32154387G>C , CM000664.2:g.32154387G>C	GRCh38
NC_000002.11:g.32379456G>C , CM000664.1:g.32379456G>C	GRCh37
NC_000002.10:g.32232960G>C	NCBI36
NG_008730.1:g.95777G>C , LRG_714:g.95777G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_014946.4:c.1742G>C MANE Select	NP_055761.2:p.Arg581Pro
ENST00000315285.9:c.1742G>C MANE Select	ENSP00000320885.3:p.Arg581Pro
NM_001363823.1:c.1739G>C	NP_001350752.1:p.Arg580Pro
NM_001363823.2:c.1739G>C	NP_001350752.1:p.Arg580Pro
NM_001363875.1:c.1643G>C	NP_001350804.1:p.Arg548Pro
NM_001363875.2:c.1643G>C	NP_001350804.1:p.Arg548Pro
NM_001377959.1:c.*15G>C	NP_001364888.1:n.*15G>C
NM_014946.3:c.1742G>C , LRG_714t1:c.1742G>C	NP_055761.2:p.Arg581Pro
NM_199436.1:c.1646G>C	NP_955468.1:p.Arg549Pro
NM_199436.2:c.1646G>C	NP_955468.1:p.Arg549Pro
ENST00000315285.7:c.1742G>C	ENSP00000320885.3:p.Arg581Pro
ENST00000345662.5:c.1646G>C	ENSP00000340817.1:p.Arg549Pro
ENST00000615843.4:c.1742G>C	ENSP00000480893.1:p.Arg581Pro
ENST00000621856.1:c.1484G>C	ENSP00000482496.1:p.Arg495Pro
ENST00000621856.2:c.1739G>C	ENSP00000482496.2:p.Arg580Pro
ENST00000642281.1:c.1479G>C
ENST00000642455.1:c.1643G>C	ENSP00000493827.1:p.Arg548Pro
ENST00000642751.1:c.1445G>C
ENST00000642999.1:c.1484G>C	ENSP00000496589.1:p.Arg495Pro
ENST00000643334.1:c.1322G>C
ENST00000644408.1:c.1641G>C
ENST00000644954.1:c.1388G>C	ENSP00000494312.1:p.Arg463Pro
ENST00000645159.1:n.2479G>C
ENST00000645671.1:c.1121G>C
ENST00000645730.1:c.921G>C
ENST00000646082.1:c.1388G>C
ENST00000646571.1:c.1646G>C	ENSP00000495015.1:p.Arg549Pro
ENST00000647007.1:n.1434G>C
ENST00000647133.1:c.1242G>C
ENST00000704289.1:c.*1402G>C	ENSP00000515816.1:n.*1402G>C
XM_005264516.3:c.1739G>C	XP_005264573.1:p.Arg580Pro
XM_005264516.5:c.1739G>C	XP_005264573.1:p.Arg580Pro
XM_011533067.1:c.*15G>C	XP_011531369.1:n.*15G>C
XM_011533067.2:c.*15G>C	XP_011531369.1:n.*15G>C
XM_017004778.2:c.*15G>C	XP_016860267.1:n.*15G>C