Canonical Allele Identifier: CA2658522781

Gene: SPAST

Linked Data

• gnomAD v4: 2-32142060-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32142060_32142061insC , CM000664.2:g.32142060_32142061insC	GRCh38
NC_000002.11:g.32367129_32367130insC , CM000664.1:g.32367129_32367130insC	GRCh37
NC_000002.10:g.32220633_32220634insC	NCBI36
NG_008730.1:g.83450_83451insC , LRG_714:g.83450_83451insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*1196+114_*1196+115insC	ENSP00000515816.1:n.*1196+114_*1196+115insC
ENST00000315285.9:c.1536+114_1536+115insC MANE Select	ENSP00000320885.3:n.1536+114_1536+115insC
ENST00000621856.2:c.1533+114_1533+115insC	ENSP00000482496.2:n.1533+114_1533+115insC
ENST00000642281.1:c.1273+114_1273+115insC
ENST00000642455.1:c.1437+114_1437+115insC	ENSP00000493827.1:n.1437+114_1437+115insC
ENST00000642751.1:c.1310+114_1310+115insC
ENST00000642999.1:c.1278+114_1278+115insC	ENSP00000496589.1:n.1278+114_1278+115insC
ENST00000643327.1:c.603+114_603+115insC
ENST00000643334.1:c.1116+114_1116+115insC
ENST00000644408.1:c.1412+114_1412+115insC
ENST00000644954.1:c.1182+114_1182+115insC	ENSP00000494312.1:n.1182+114_1182+115insC
ENST00000645159.1:n.2273+114_2273+115insC
ENST00000645671.1:c.986+114_986+115insC
ENST00000645730.1:c.715+114_715+115insC
ENST00000646082.1:c.1182+114_1182+115insC
ENST00000646571.1:c.1440+114_1440+115insC	ENSP00000495015.1:n.1440+114_1440+115insC
ENST00000647007.1:n.1228+114_1228+115insC
ENST00000647133.1:c.1036+114_1036+115insC
ENST00000315285.7:c.1536+114_1536+115insC	ENSP00000320885.3:n.1536+114_1536+115insC
ENST00000345662.5:c.1440+114_1440+115insC	ENSP00000340817.1:n.1440+114_1440+115insC
ENST00000615843.4:c.1536+114_1536+115insC	ENSP00000480893.1:n.1536+114_1536+115insC
ENST00000621856.1:c.1278+114_1278+115insC	ENSP00000482496.1:n.1278+114_1278+115insC
NM_014946.3:c.1536+114_1536+115insC , LRG_714t1:c.1536+114_1536+115insC	NP_055761.2:n.1536+114_1536+115insC
NM_199436.1:c.1440+114_1440+115insC	NP_955468.1:n.1440+114_1440+115insC
XM_005264516.3:c.1533+114_1533+115insC	XP_005264573.1:n.1533+114_1533+115insC
XM_011533067.1:c.1536+114_1536+115insC	XP_011531369.1:n.1536+114_1536+115insC
NM_001363823.1:c.1533+114_1533+115insC	NP_001350752.1:n.1533+114_1533+115insC
NM_001363875.1:c.1437+114_1437+115insC	NP_001350804.1:n.1437+114_1437+115insC
XM_005264516.5:c.1533+114_1533+115insC	XP_005264573.1:n.1533+114_1533+115insC
XM_011533067.2:c.1536+114_1536+115insC	XP_011531369.1:n.1536+114_1536+115insC
XM_017004778.2:c.1440+114_1440+115insC	XP_016860267.1:n.1440+114_1440+115insC
NM_001363823.2:c.1533+114_1533+115insC	NP_001350752.1:n.1533+114_1533+115insC
NM_001363875.2:c.1437+114_1437+115insC	NP_001350804.1:n.1437+114_1437+115insC
NM_001377959.1:c.1440+114_1440+115insC	NP_001364888.1:n.1440+114_1440+115insC
NM_014946.4:c.1536+114_1536+115insC MANE Select	NP_055761.2:n.1536+114_1536+115insC
NM_199436.2:c.1440+114_1440+115insC	NP_955468.1:n.1440+114_1440+115insC