Canonical Allele Identifier: CA2658529177

Gene: SPAST

Linked Data

• gnomAD v4: 2-32136697-A-ATTT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32136697_32136698insTTT , CM000664.2:g.32136697_32136698insTTT	GRCh38
NC_000002.11:g.32361766_32361767insTTT , CM000664.1:g.32361766_32361767insTTT	GRCh37
NC_000002.10:g.32215270_32215271insTTT	NCBI36
NG_008730.1:g.78087_78088insTTT , LRG_714:g.78087_78088insTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*981+59_*981+60insTTT	ENSP00000515816.1:n.*981+59_*981+60insTTT
ENST00000315285.9:c.1321+59_1321+60insTTT MANE Select	ENSP00000320885.3:n.1321+59_1321+60insTTT
ENST00000621856.2:c.1318+59_1318+60insTTT	ENSP00000482496.2:n.1318+59_1318+60insTTT
ENST00000642281.1:c.1058+59_1058+60insTTT
ENST00000642455.1:c.1222+59_1222+60insTTT	ENSP00000493827.1:n.1222+59_1222+60insTTT
ENST00000642751.1:c.1095+59_1095+60insTTT
ENST00000642999.1:c.1063+59_1063+60insTTT	ENSP00000496589.1:n.1063+59_1063+60insTTT
ENST00000643327.1:c.480+59_480+60insTTT
ENST00000643334.1:c.901+59_901+60insTTT
ENST00000644408.1:c.1197+59_1197+60insTTT
ENST00000644954.1:c.967+59_967+60insTTT	ENSP00000494312.1:n.967+59_967+60insTTT
ENST00000645159.1:n.2058+59_2058+60insTTT
ENST00000645671.1:c.771+59_771+60insTTT
ENST00000645730.1:c.593-412_593-411insTTT
ENST00000646082.1:c.967+59_967+60insTTT
ENST00000646571.1:c.1225+59_1225+60insTTT	ENSP00000495015.1:n.1225+59_1225+60insTTT
ENST00000647007.1:n.1013+59_1013+60insTTT
ENST00000647133.1:c.821+59_821+60insTTT
ENST00000315285.7:c.1321+59_1321+60insTTT	ENSP00000320885.3:n.1321+59_1321+60insTTT
ENST00000345662.5:c.1225+59_1225+60insTTT	ENSP00000340817.1:n.1225+59_1225+60insTTT
ENST00000615843.4:c.1321+59_1321+60insTTT	ENSP00000480893.1:n.1321+59_1321+60insTTT
ENST00000621856.1:c.1063+59_1063+60insTTT	ENSP00000482496.1:n.1063+59_1063+60insTTT
NM_014946.3:c.1321+59_1321+60insTTT , LRG_714t1:c.1321+59_1321+60insTTT	NP_055761.2:n.1321+59_1321+60insTTT
NM_199436.1:c.1225+59_1225+60insTTT	NP_955468.1:n.1225+59_1225+60insTTT
XM_005264516.3:c.1318+59_1318+60insTTT	XP_005264573.1:n.1318+59_1318+60insTTT
XM_011533067.1:c.1321+59_1321+60insTTT	XP_011531369.1:n.1321+59_1321+60insTTT
NM_001363823.1:c.1318+59_1318+60insTTT	NP_001350752.1:n.1318+59_1318+60insTTT
NM_001363875.1:c.1222+59_1222+60insTTT	NP_001350804.1:n.1222+59_1222+60insTTT
XM_005264516.5:c.1318+59_1318+60insTTT	XP_005264573.1:n.1318+59_1318+60insTTT
XM_011533067.2:c.1321+59_1321+60insTTT	XP_011531369.1:n.1321+59_1321+60insTTT
XM_017004778.2:c.1225+59_1225+60insTTT	XP_016860267.1:n.1225+59_1225+60insTTT
NM_001363823.2:c.1318+59_1318+60insTTT	NP_001350752.1:n.1318+59_1318+60insTTT
NM_001363875.2:c.1222+59_1222+60insTTT	NP_001350804.1:n.1222+59_1222+60insTTT
NM_001377959.1:c.1225+59_1225+60insTTT	NP_001364888.1:n.1225+59_1225+60insTTT
NM_014946.4:c.1321+59_1321+60insTTT MANE Select	NP_055761.2:n.1321+59_1321+60insTTT
NM_199436.2:c.1225+59_1225+60insTTT	NP_955468.1:n.1225+59_1225+60insTTT