Canonical Allele Identifier: CA346501300

Gene: SPAST

Linked Data

• MyVariant Identifiers: chr2:g.32352068C>A (hg19) ; chr2:g.32126999C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32126999C>A , CM000664.2:g.32126999C>A	GRCh38
NC_000002.11:g.32352068C>A , CM000664.1:g.32352068C>A	GRCh37
NC_000002.10:g.32205572C>A	NCBI36
NG_008730.1:g.68389C>A , LRG_714:g.68389C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*810C>A	ENSP00000515816.1:n.*810C>A
ENST00000315285.9:c.1150C>A MANE Select	ENSP00000320885.3:p.Pro384Thr
ENST00000621856.2:c.1147C>A	ENSP00000482496.2:p.Pro383Thr
ENST00000642281.1:c.983-9564C>A
ENST00000642455.1:c.1051C>A	ENSP00000493827.1:p.Pro351Thr
ENST00000642751.1:c.924C>A
ENST00000642999.1:c.892C>A	ENSP00000496589.1:p.Pro298Thr
ENST00000643327.1:c.309C>A
ENST00000643334.1:c.730C>A
ENST00000644408.1:c.1026C>A
ENST00000644954.1:c.796C>A	ENSP00000494312.1:p.Pro266Thr
ENST00000645159.1:n.502C>A
ENST00000645550.1:n.363C>A
ENST00000645671.1:c.600C>A
ENST00000645730.1:c.497C>A
ENST00000646082.1:c.796C>A
ENST00000646571.1:c.1054C>A	ENSP00000495015.1:p.Pro352Thr
ENST00000647007.1:n.842C>A
ENST00000647133.1:c.674-1409C>A
ENST00000315285.7:c.1150C>A	ENSP00000320885.3:p.Pro384Thr
ENST00000345662.5:c.1054C>A	ENSP00000340817.1:p.Pro352Thr
ENST00000615843.4:c.1150C>A	ENSP00000480893.1:p.Pro384Thr
ENST00000621856.1:c.892C>A	ENSP00000482496.1:p.Pro298Thr
NM_014946.3:c.1150C>A , LRG_714t1:c.1150C>A	NP_055761.2:p.Pro384Thr
NM_199436.1:c.1054C>A	NP_955468.1:p.Pro352Thr
XM_005264516.3:c.1147C>A	XP_005264573.1:p.Pro383Thr
XM_011533067.1:c.1150C>A	XP_011531369.1:p.Pro384Thr
NM_001363823.1:c.1147C>A	NP_001350752.1:p.Pro383Thr
NM_001363875.1:c.1051C>A	NP_001350804.1:p.Pro351Thr
XM_005264516.5:c.1147C>A	XP_005264573.1:p.Pro383Thr
XM_011533067.2:c.1150C>A	XP_011531369.1:p.Pro384Thr
XM_017004778.2:c.1054C>A	XP_016860267.1:p.Pro352Thr
NM_001363823.2:c.1147C>A	NP_001350752.1:p.Pro383Thr
NM_001363875.2:c.1051C>A	NP_001350804.1:p.Pro351Thr
NM_001377959.1:c.1054C>A	NP_001364888.1:p.Pro352Thr
NM_014946.4:c.1150C>A MANE Select	NP_055761.2:p.Pro384Thr
NM_199436.2:c.1054C>A	NP_955468.1:p.Pro352Thr