Canonical Allele Identifier: CA1242498132

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32128445_32128450delinsTTAATA , CM000664.2:g.32128445_32128450delinsTTAATA	GRCh38
NC_000002.11:g.32353514_32353519delinsTTAATA , CM000664.1:g.32353514_32353519delinsTTAATA	GRCh37
NC_000002.10:g.32207018_32207023delinsTTAATA	NCBI36
NG_008730.1:g.69835_69840delinsTTAATA , LRG_714:g.69835_69840delinsTTAATA

Transcript Alleles

HGVS	Amino-acid change
ENST00000704289.1:c.*871_*876delinsTTAATA	ENSP00000515816.1:n.*871_*876delinsTTAATA...
ENST00000315285.9:c.1211_1216delinsTTAATA MANE Select	ENSP00000320885.3:p.Phe404=
ENST00000621856.2:c.1208_1213delinsTTAATA	ENSP00000482496.2:p.Phe403=
ENST00000642281.1:c.983-8118_983-8113delinsTTAATA
ENST00000642455.1:c.1112_1117delinsTTAATA	ENSP00000493827.1:p.Phe371=
ENST00000642751.1:c.985_990delinsTTAATA
ENST00000642999.1:c.953_958delinsTTAATA	ENSP00000496589.1:p.Phe318=
ENST00000643327.1:c.370_375delinsTTAATA
ENST00000643334.1:c.791_796delinsTTAATA
ENST00000644408.1:c.1087_1092delinsTTAATA
ENST00000644954.1:c.857_862delinsTTAATA	ENSP00000494312.1:p.Phe286=
ENST00000645159.1:n.1948_1953delinsTTAATA
ENST00000645550.1:n.424_429delinsTTAATA
ENST00000645671.1:c.661_666delinsTTAATA
ENST00000645730.1:c.558_563delinsTTAATA
ENST00000646082.1:c.857_862delinsTTAATA
ENST00000646571.1:c.1115_1120delinsTTAATA	ENSP00000495015.1:p.Phe372=
ENST00000647007.1:n.903_908delinsTTAATA
ENST00000647133.1:c.711_716delinsTTAATA
ENST00000315285.7:c.1211_1216delinsTTAATA	ENSP00000320885.3:p.Phe404=
ENST00000345662.5:c.1115_1120delinsTTAATA	ENSP00000340817.1:p.Phe372=
ENST00000615843.4:c.1211_1216delinsTTAATA	ENSP00000480893.1:p.Phe404=
ENST00000621856.1:c.953_958delinsTTAATA	ENSP00000482496.1:p.Phe318=
NM_014946.3:c.1211_1216delinsTTAATA , LRG_714t1:c.1211_1216delinsTTAATA	NP_055761.2:p.Phe404=
NM_199436.1:c.1115_1120delinsTTAATA	NP_955468.1:p.Phe372=
XM_005264516.3:c.1208_1213delinsTTAATA	XP_005264573.1:p.Phe403=
XM_011533067.1:c.1211_1216delinsTTAATA	XP_011531369.1:p.Phe404=
NM_001363823.1:c.1208_1213delinsTTAATA	NP_001350752.1:p.Phe403=
NM_001363875.1:c.1112_1117delinsTTAATA	NP_001350804.1:p.Phe371=
XM_005264516.5:c.1208_1213delinsTTAATA	XP_005264573.1:p.Phe403=
XM_011533067.2:c.1211_1216delinsTTAATA	XP_011531369.1:p.Phe404=
XM_017004778.2:c.1115_1120delinsTTAATA	XP_016860267.1:p.Phe372=
NM_001363823.2:c.1208_1213delinsTTAATA	NP_001350752.1:p.Phe403=
NM_001363875.2:c.1112_1117delinsTTAATA	NP_001350804.1:p.Phe371=
NM_001377959.1:c.1115_1120delinsTTAATA	NP_001364888.1:p.Phe372=
NM_014946.4:c.1211_1216delinsTTAATA MANE Select	NP_055761.2:p.Phe404=
NM_199436.2:c.1115_1120delinsTTAATA	NP_955468.1:p.Phe372=