Canonical Allele Identifier: CA2658521772

Gene: SPAST

Linked Data

• gnomAD v4: 2-32089395-C-CAT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32089395_32089396insAT , CM000664.2:g.32089395_32089396insAT	GRCh38
NC_000002.11:g.32314464_32314465insAT , CM000664.1:g.32314464_32314465insAT	GRCh37
NC_000002.10:g.32167968_32167969insAT	NCBI36
NG_008730.1:g.30785_30786insAT , LRG_714:g.30785_30786insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*163-127_*163-126insAT	ENSP00000515816.1:n.*163-127_*163-126insAT
ENST00000315285.9:c.503-127_503-126insAT MANE Select	ENSP00000320885.3:n.503-127_503-126insAT
ENST00000621856.2:c.500-127_500-126insAT	ENSP00000482496.2:n.500-127_500-126insAT
ENST00000642281.1:c.387-127_387-126insAT
ENST00000642455.1:c.500-127_500-126insAT	ENSP00000493827.1:n.500-127_500-126insAT
ENST00000642751.1:c.373-127_373-126insAT
ENST00000642999.1:c.245-127_245-126insAT	ENSP00000496589.1:n.245-127_245-126insAT
ENST00000643334.1:c.88-127_88-126insAT
ENST00000644408.1:c.379-127_379-126insAT
ENST00000644954.1:c.245-127_245-126insAT	ENSP00000494312.1:n.245-127_245-126insAT
ENST00000645400.1:c.459-127_459-126insAT	ENSP00000496306.1:n.459-127_459-126insAT
ENST00000645671.1:c.37-9401_37-9400insAT
ENST00000646082.1:c.337-127_337-126insAT
ENST00000646571.1:c.503-127_503-126insAT	ENSP00000495015.1:n.503-127_503-126insAT
ENST00000647007.1:n.200-127_200-126insAT
ENST00000647133.1:c.78-127_78-126insAT
ENST00000315285.7:c.503-127_503-126insAT	ENSP00000320885.3:n.503-127_503-126insAT
ENST00000345662.5:c.503-127_503-126insAT	ENSP00000340817.1:n.503-127_503-126insAT
ENST00000615843.4:c.503-127_503-126insAT	ENSP00000480893.1:n.503-127_503-126insAT
ENST00000621856.1:c.245-127_245-126insAT	ENSP00000482496.1:n.245-127_245-126insAT
NM_014946.3:c.503-127_503-126insAT , LRG_714t1:c.503-127_503-126insAT	NP_055761.2:n.503-127_503-126insAT
NM_199436.1:c.503-127_503-126insAT	NP_955468.1:n.503-127_503-126insAT
XM_005264516.3:c.500-127_500-126insAT	XP_005264573.1:n.500-127_500-126insAT
XM_011533067.1:c.503-127_503-126insAT	XP_011531369.1:n.503-127_503-126insAT
NM_001363823.1:c.500-127_500-126insAT	NP_001350752.1:n.500-127_500-126insAT
NM_001363875.1:c.500-127_500-126insAT	NP_001350804.1:n.500-127_500-126insAT
XM_005264516.5:c.500-127_500-126insAT	XP_005264573.1:n.500-127_500-126insAT
XM_011533067.2:c.503-127_503-126insAT	XP_011531369.1:n.503-127_503-126insAT
XM_017004778.2:c.503-127_503-126insAT	XP_016860267.1:n.503-127_503-126insAT
NM_001363823.2:c.500-127_500-126insAT	NP_001350752.1:n.500-127_500-126insAT
NM_001363875.2:c.500-127_500-126insAT	NP_001350804.1:n.500-127_500-126insAT
NM_001377959.1:c.503-127_503-126insAT	NP_001364888.1:n.503-127_503-126insAT
NM_014946.4:c.503-127_503-126insAT MANE Select	NP_055761.2:n.503-127_503-126insAT
NM_199436.2:c.503-127_503-126insAT	NP_955468.1:n.503-127_503-126insAT