Canonical Allele Identifier: CA1242498127

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32128440_32128444delinsCTTCT , CM000664.2:g.32128440_32128444delinsCTTCT	GRCh38
NC_000002.11:g.32353509_32353513delinsCTTCT , CM000664.1:g.32353509_32353513delinsCTTCT	GRCh37
NC_000002.10:g.32207013_32207017delinsCTTCT	NCBI36
NG_008730.1:g.69830_69834delinsCTTCT , LRG_714:g.69830_69834delinsCTTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*866_*870delinsCTTCT	ENSP00000515816.1:n.*866_*870delinsCTTCT
ENST00000315285.9:c.1206_1210delinsCTTCT MANE Select	ENSP00000320885.3:p.Thr402=
ENST00000621856.2:c.1203_1207delinsCTTCT	ENSP00000482496.2:p.Thr401=
ENST00000642281.1:c.983-8123_983-8119delinsCTTCT
ENST00000642455.1:c.1107_1111delinsCTTCT	ENSP00000493827.1:p.Thr369=
ENST00000642751.1:c.980_984delinsCTTCT
ENST00000642999.1:c.948_952delinsCTTCT	ENSP00000496589.1:p.Thr316=
ENST00000643327.1:c.365_369delinsCTTCT
ENST00000643334.1:c.786_790delinsCTTCT
ENST00000644408.1:c.1082_1086delinsCTTCT
ENST00000644954.1:c.852_856delinsCTTCT	ENSP00000494312.1:p.Thr284=
ENST00000645159.1:n.1943_1947delinsCTTCT
ENST00000645550.1:n.419_423delinsCTTCT
ENST00000645671.1:c.656_660delinsCTTCT
ENST00000645730.1:c.553_557delinsCTTCT
ENST00000646082.1:c.852_856delinsCTTCT
ENST00000646571.1:c.1110_1114delinsCTTCT	ENSP00000495015.1:p.Thr370=
ENST00000647007.1:n.898_902delinsCTTCT
ENST00000647133.1:c.706_710delinsCTTCT
ENST00000315285.7:c.1206_1210delinsCTTCT	ENSP00000320885.3:p.Thr402=
ENST00000345662.5:c.1110_1114delinsCTTCT	ENSP00000340817.1:p.Thr370=
ENST00000615843.4:c.1206_1210delinsCTTCT	ENSP00000480893.1:p.Thr402=
ENST00000621856.1:c.948_952delinsCTTCT	ENSP00000482496.1:p.Thr316=
NM_014946.3:c.1206_1210delinsCTTCT , LRG_714t1:c.1206_1210delinsCTTCT	NP_055761.2:p.Thr402=
NM_199436.1:c.1110_1114delinsCTTCT	NP_955468.1:p.Thr370=
XM_005264516.3:c.1203_1207delinsCTTCT	XP_005264573.1:p.Thr401=
XM_011533067.1:c.1206_1210delinsCTTCT	XP_011531369.1:p.Thr402=
NM_001363823.1:c.1203_1207delinsCTTCT	NP_001350752.1:p.Thr401=
NM_001363875.1:c.1107_1111delinsCTTCT	NP_001350804.1:p.Thr369=
XM_005264516.5:c.1203_1207delinsCTTCT	XP_005264573.1:p.Thr401=
XM_011533067.2:c.1206_1210delinsCTTCT	XP_011531369.1:p.Thr402=
XM_017004778.2:c.1110_1114delinsCTTCT	XP_016860267.1:p.Thr370=
NM_001363823.2:c.1203_1207delinsCTTCT	NP_001350752.1:p.Thr401=
NM_001363875.2:c.1107_1111delinsCTTCT	NP_001350804.1:p.Thr369=
NM_001377959.1:c.1110_1114delinsCTTCT	NP_001364888.1:p.Thr370=
NM_014946.4:c.1206_1210delinsCTTCT MANE Select	NP_055761.2:p.Thr402=
NM_199436.2:c.1110_1114delinsCTTCT	NP_955468.1:p.Thr370=