Canonical Allele Identifier: CA1242461777

Gene: SPAST

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32064148_32064154delinsCGCCGGT , CM000664.2:g.32064148_32064154delinsCGCCGGT	GRCh38
NC_000002.11:g.32289217_32289223delinsCGCCGGT , CM000664.1:g.32289217_32289223delinsCGCCGGT	GRCh37
NC_000002.10:g.32142721_32142727delinsCGCCGGT	NCBI36
NG_008730.1:g.5538_5544delinsCGCCGGT , LRG_714:g.5538_5544delinsCGCCGGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000704289.1:c.317_323delinsCGCCGGT	ENSP00000515816.1:p.Ala106=
ENST00000315285.9:c.317_323delinsCGCCGGT MANE Select	ENSP00000320885.3:p.Ala106=
ENST00000621856.2:c.317_323delinsCGCCGGT	ENSP00000482496.2:p.Ala106=
ENST00000642281.1:c.201_207delinsCGCCGGT
ENST00000642455.1:c.317_323delinsCGCCGGT	ENSP00000493827.1:p.Ala106=
ENST00000642751.1:c.187_193delinsCGCCGGT
ENST00000642999.1:c.59_65delinsCGCCGGT	ENSP00000496589.1:p.Ala20=
ENST00000644408.1:c.193_199delinsCGCCGGT
ENST00000644954.1:c.59_65delinsCGCCGGT	ENSP00000494312.1:p.Ala20=
ENST00000645400.1:c.158_164delinsCGCCGGT	ENSP00000496306.1:p.Ala53=
ENST00000646082.1:c.151_157delinsCGCCGGT
ENST00000646571.1:c.317_323delinsCGCCGGT	ENSP00000495015.1:p.Ala106=
ENST00000315285.7:c.317_323delinsCGCCGGT	ENSP00000320885.3:p.Ala106=
ENST00000345662.5:c.317_323delinsCGCCGGT	ENSP00000340817.1:p.Ala106=
ENST00000615843.4:c.317_323delinsCGCCGGT	ENSP00000480893.1:p.Ala106=
ENST00000621856.1:c.59_65delinsCGCCGGT	ENSP00000482496.1:p.Ala20=
NM_014946.3:c.317_323delinsCGCCGGT , LRG_714t1:c.317_323delinsCGCCGGT	NP_055761.2:p.Ala106=
NM_199436.1:c.317_323delinsCGCCGGT	NP_955468.1:p.Ala106=
XM_005264516.3:c.317_323delinsCGCCGGT	XP_005264573.1:p.Ala106=
XM_011533067.1:c.317_323delinsCGCCGGT	XP_011531369.1:p.Ala106=
NM_001363823.1:c.317_323delinsCGCCGGT	NP_001350752.1:p.Ala106=
NM_001363875.1:c.317_323delinsCGCCGGT	NP_001350804.1:p.Ala106=
XM_005264516.5:c.317_323delinsCGCCGGT	XP_005264573.1:p.Ala106=
XM_011533067.2:c.317_323delinsCGCCGGT	XP_011531369.1:p.Ala106=
XM_017004778.2:c.317_323delinsCGCCGGT	XP_016860267.1:p.Ala106=
NM_001363823.2:c.317_323delinsCGCCGGT	NP_001350752.1:p.Ala106=
NM_001363875.2:c.317_323delinsCGCCGGT	NP_001350804.1:p.Ala106=
NM_001377959.1:c.317_323delinsCGCCGGT	NP_001364888.1:p.Ala106=
NM_014946.4:c.317_323delinsCGCCGGT MANE Select	NP_055761.2:p.Ala106=
NM_199436.2:c.317_323delinsCGCCGGT	NP_955468.1:p.Ala106=