Canonical Allele Identifier: CA425448620

Gene: SPAST

Linked Data

• MyVariant Identifiers: chr2:g.32361691T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32136622T>A , CM000664.2:g.32136622T>A	GRCh38
NC_000002.11:g.32361691T>A , CM000664.1:g.32361691T>A	GRCh37
NC_000002.10:g.32215195T>A	NCBI36
NG_008730.1:g.78012T>A , LRG_714:g.78012T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000704289.1:c.*965T>A	ENSP00000515816.1:n.*965T>A
ENST00000315285.9:c.1305T>A MANE Select	ENSP00000320885.3:p.Pro435=
ENST00000621856.2:c.1302T>A	ENSP00000482496.2:p.Pro434=
ENST00000642281.1:c.1042T>A
ENST00000642455.1:c.1206T>A	ENSP00000493827.1:p.Pro402=
ENST00000642751.1:c.1079T>A
ENST00000642999.1:c.1047T>A	ENSP00000496589.1:p.Pro349=
ENST00000643327.1:c.464T>A
ENST00000643334.1:c.885T>A
ENST00000644408.1:c.1181T>A
ENST00000644954.1:c.951T>A	ENSP00000494312.1:p.Pro317=
ENST00000645159.1:n.2042T>A
ENST00000645671.1:c.755T>A
ENST00000645730.1:c.593-487T>A
ENST00000646082.1:c.951T>A
ENST00000646571.1:c.1209T>A	ENSP00000495015.1:p.Pro403=
ENST00000647007.1:n.997T>A
ENST00000647133.1:c.805T>A
ENST00000315285.7:c.1305T>A	ENSP00000320885.3:p.Pro435=
ENST00000345662.5:c.1209T>A	ENSP00000340817.1:p.Pro403=
ENST00000615843.4:c.1305T>A	ENSP00000480893.1:p.Pro435=
ENST00000621856.1:c.1047T>A	ENSP00000482496.1:p.Pro349=
NM_014946.3:c.1305T>A , LRG_714t1:c.1305T>A	NP_055761.2:p.Pro435=
NM_199436.1:c.1209T>A	NP_955468.1:p.Pro403=
XM_005264516.3:c.1302T>A	XP_005264573.1:p.Pro434=
XM_011533067.1:c.1305T>A	XP_011531369.1:p.Pro435=
NM_001363823.1:c.1302T>A	NP_001350752.1:p.Pro434=
NM_001363875.1:c.1206T>A	NP_001350804.1:p.Pro402=
XM_005264516.5:c.1302T>A	XP_005264573.1:p.Pro434=
XM_011533067.2:c.1305T>A	XP_011531369.1:p.Pro435=
XM_017004778.2:c.1209T>A	XP_016860267.1:p.Pro403=
NM_001363823.2:c.1302T>A	NP_001350752.1:p.Pro434=
NM_001363875.2:c.1206T>A	NP_001350804.1:p.Pro402=
NM_001377959.1:c.1209T>A	NP_001364888.1:p.Pro403=
NM_014946.4:c.1305T>A MANE Select	NP_055761.2:p.Pro435=
NM_199436.2:c.1209T>A	NP_955468.1:p.Pro403=