Canonical Allele Identifier: CA1600811

Gene: SPAST

Linked Data

• dbSNP Id: rs778978064
• ExAC: 2:32352079 G / C
• gnomAD v4: 2-32127010-G-C
• MyVariant Identifiers: chr2:g.32352079G>C (hg19) ; chr2:g.32127010G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32127010G>C , CM000664.2:g.32127010G>C	GRCh38
NC_000002.11:g.32352079G>C , CM000664.1:g.32352079G>C	GRCh37
NC_000002.10:g.32205583G>C	NCBI36
NG_008730.1:g.68400G>C , LRG_714:g.68400G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*821G>C	ENSP00000515816.1:n.*821G>C
ENST00000315285.9:c.1161G>C MANE Select	ENSP00000320885.3:p.Gly387=
ENST00000621856.2:c.1158G>C	ENSP00000482496.2:p.Gly386=
ENST00000642281.1:c.983-9553G>C
ENST00000642455.1:c.1062G>C	ENSP00000493827.1:p.Gly354=
ENST00000642751.1:c.935G>C
ENST00000642999.1:c.903G>C	ENSP00000496589.1:p.Gly301=
ENST00000643327.1:c.320G>C
ENST00000643334.1:c.741G>C
ENST00000644408.1:c.1037G>C
ENST00000644954.1:c.807G>C	ENSP00000494312.1:p.Gly269=
ENST00000645159.1:n.513G>C
ENST00000645550.1:n.374G>C
ENST00000645671.1:c.611G>C
ENST00000645730.1:c.508G>C
ENST00000646082.1:c.807G>C
ENST00000646571.1:c.1065G>C	ENSP00000495015.1:p.Gly355=
ENST00000647007.1:n.853G>C
ENST00000647133.1:c.674-1398G>C
ENST00000315285.7:c.1161G>C	ENSP00000320885.3:p.Gly387=
ENST00000345662.5:c.1065G>C	ENSP00000340817.1:p.Gly355=
ENST00000615843.4:c.1161G>C	ENSP00000480893.1:p.Gly387=
ENST00000621856.1:c.903G>C	ENSP00000482496.1:p.Gly301=
NM_014946.3:c.1161G>C , LRG_714t1:c.1161G>C	NP_055761.2:p.Gly387=
NM_199436.1:c.1065G>C	NP_955468.1:p.Gly355=
XM_005264516.3:c.1158G>C	XP_005264573.1:p.Gly386=
XM_011533067.1:c.1161G>C	XP_011531369.1:p.Gly387=
NM_001363823.1:c.1158G>C	NP_001350752.1:p.Gly386=
NM_001363875.1:c.1062G>C	NP_001350804.1:p.Gly354=
XM_005264516.5:c.1158G>C	XP_005264573.1:p.Gly386=
XM_011533067.2:c.1161G>C	XP_011531369.1:p.Gly387=
XM_017004778.2:c.1065G>C	XP_016860267.1:p.Gly355=
NM_001363823.2:c.1158G>C	NP_001350752.1:p.Gly386=
NM_001363875.2:c.1062G>C	NP_001350804.1:p.Gly354=
NM_001377959.1:c.1065G>C	NP_001364888.1:p.Gly355=
NM_014946.4:c.1161G>C MANE Select	NP_055761.2:p.Gly387=
NM_199436.2:c.1065G>C	NP_955468.1:p.Gly355=