Canonical Allele Identifier: CA346502118

Gene: SPAST

Linked Data

• MyVariant Identifiers: chr2:g.32361696T>C (hg19) ; chr2:g.32136627T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32136627T>C , CM000664.2:g.32136627T>C	GRCh38
NC_000002.11:g.32361696T>C , CM000664.1:g.32361696T>C	GRCh37
NC_000002.10:g.32215200T>C	NCBI36
NG_008730.1:g.78017T>C , LRG_714:g.78017T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*970T>C	ENSP00000515816.1:n.*970T>C
ENST00000315285.9:c.1310T>C MANE Select	ENSP00000320885.3:p.Ile437Thr
ENST00000621856.2:c.1307T>C	ENSP00000482496.2:p.Ile436Thr
ENST00000642281.1:c.1047T>C
ENST00000642455.1:c.1211T>C	ENSP00000493827.1:p.Ile404Thr
ENST00000642751.1:c.1084T>C
ENST00000642999.1:c.1052T>C	ENSP00000496589.1:p.Ile351Thr
ENST00000643327.1:c.469T>C
ENST00000643334.1:c.890T>C
ENST00000644408.1:c.1186T>C
ENST00000644954.1:c.956T>C	ENSP00000494312.1:p.Ile319Thr
ENST00000645159.1:n.2047T>C
ENST00000645671.1:c.760T>C
ENST00000645730.1:c.593-482T>C
ENST00000646082.1:c.956T>C
ENST00000646571.1:c.1214T>C	ENSP00000495015.1:p.Ile405Thr
ENST00000647007.1:n.1002T>C
ENST00000647133.1:c.810T>C
ENST00000315285.7:c.1310T>C	ENSP00000320885.3:p.Ile437Thr
ENST00000345662.5:c.1214T>C	ENSP00000340817.1:p.Ile405Thr
ENST00000615843.4:c.1310T>C	ENSP00000480893.1:p.Ile437Thr
ENST00000621856.1:c.1052T>C	ENSP00000482496.1:p.Ile351Thr
NM_014946.3:c.1310T>C , LRG_714t1:c.1310T>C	NP_055761.2:p.Ile437Thr
NM_199436.1:c.1214T>C	NP_955468.1:p.Ile405Thr
XM_005264516.3:c.1307T>C	XP_005264573.1:p.Ile436Thr
XM_011533067.1:c.1310T>C	XP_011531369.1:p.Ile437Thr
NM_001363823.1:c.1307T>C	NP_001350752.1:p.Ile436Thr
NM_001363875.1:c.1211T>C	NP_001350804.1:p.Ile404Thr
XM_005264516.5:c.1307T>C	XP_005264573.1:p.Ile436Thr
XM_011533067.2:c.1310T>C	XP_011531369.1:p.Ile437Thr
XM_017004778.2:c.1214T>C	XP_016860267.1:p.Ile405Thr
NM_001363823.2:c.1307T>C	NP_001350752.1:p.Ile436Thr
NM_001363875.2:c.1211T>C	NP_001350804.1:p.Ile404Thr
NM_001377959.1:c.1214T>C	NP_001364888.1:p.Ile405Thr
NM_014946.4:c.1310T>C MANE Select	NP_055761.2:p.Ile437Thr
NM_199436.2:c.1214T>C	NP_955468.1:p.Ile405Thr