Canonical Allele Identifier: CA1242498125

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32128439_32128442delinsCCTT , CM000664.2:g.32128439_32128442delinsCCTT	GRCh38
NC_000002.11:g.32353508_32353511delinsCCTT , CM000664.1:g.32353508_32353511delinsCCTT	GRCh37
NC_000002.10:g.32207012_32207015delinsCCTT	NCBI36
NG_008730.1:g.69829_69832delinsCCTT , LRG_714:g.69829_69832delinsCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*865_*868delinsCCTT	ENSP00000515816.1:n.*865_*868delinsCCTT
ENST00000315285.9:c.1205_1208delinsCCTT MANE Select	ENSP00000320885.3:p.Thr402=
ENST00000621856.2:c.1202_1205delinsCCTT	ENSP00000482496.2:p.Thr401=
ENST00000642281.1:c.983-8124_983-8121delinsCCTT
ENST00000642455.1:c.1106_1109delinsCCTT	ENSP00000493827.1:p.Thr369=
ENST00000642751.1:c.979_982delinsCCTT
ENST00000642999.1:c.947_950delinsCCTT	ENSP00000496589.1:p.Thr316=
ENST00000643327.1:c.364_367delinsCCTT
ENST00000643334.1:c.785_788delinsCCTT
ENST00000644408.1:c.1081_1084delinsCCTT
ENST00000644954.1:c.851_854delinsCCTT	ENSP00000494312.1:p.Thr284=
ENST00000645159.1:n.1942_1945delinsCCTT
ENST00000645550.1:n.418_421delinsCCTT
ENST00000645671.1:c.655_658delinsCCTT
ENST00000645730.1:c.552_555delinsCCTT
ENST00000646082.1:c.851_854delinsCCTT
ENST00000646571.1:c.1109_1112delinsCCTT	ENSP00000495015.1:p.Thr370=
ENST00000647007.1:n.897_900delinsCCTT
ENST00000647133.1:c.705_708delinsCCTT
ENST00000315285.7:c.1205_1208delinsCCTT	ENSP00000320885.3:p.Thr402=
ENST00000345662.5:c.1109_1112delinsCCTT	ENSP00000340817.1:p.Thr370=
ENST00000615843.4:c.1205_1208delinsCCTT	ENSP00000480893.1:p.Thr402=
ENST00000621856.1:c.947_950delinsCCTT	ENSP00000482496.1:p.Thr316=
NM_014946.3:c.1205_1208delinsCCTT , LRG_714t1:c.1205_1208delinsCCTT	NP_055761.2:p.Thr402=
NM_199436.1:c.1109_1112delinsCCTT	NP_955468.1:p.Thr370=
XM_005264516.3:c.1202_1205delinsCCTT	XP_005264573.1:p.Thr401=
XM_011533067.1:c.1205_1208delinsCCTT	XP_011531369.1:p.Thr402=
NM_001363823.1:c.1202_1205delinsCCTT	NP_001350752.1:p.Thr401=
NM_001363875.1:c.1106_1109delinsCCTT	NP_001350804.1:p.Thr369=
XM_005264516.5:c.1202_1205delinsCCTT	XP_005264573.1:p.Thr401=
XM_011533067.2:c.1205_1208delinsCCTT	XP_011531369.1:p.Thr402=
XM_017004778.2:c.1109_1112delinsCCTT	XP_016860267.1:p.Thr370=
NM_001363823.2:c.1202_1205delinsCCTT	NP_001350752.1:p.Thr401=
NM_001363875.2:c.1106_1109delinsCCTT	NP_001350804.1:p.Thr369=
NM_001377959.1:c.1109_1112delinsCCTT	NP_001364888.1:p.Thr370=
NM_014946.4:c.1205_1208delinsCCTT MANE Select	NP_055761.2:p.Thr402=
NM_199436.2:c.1109_1112delinsCCTT	NP_955468.1:p.Thr370=