Canonical Allele Identifier: CA425449190

Gene: SPAST

Linked Data

• MyVariant Identifiers: chr2:g.32362207T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32137138T>C , CM000664.2:g.32137138T>C	GRCh38
NC_000002.11:g.32362207T>C , CM000664.1:g.32362207T>C	GRCh37
NC_000002.10:g.32215711T>C	NCBI36
NG_008730.1:g.78528T>C , LRG_714:g.78528T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000704289.1:c.*1103T>C	ENSP00000515816.1:n.*1103T>C
ENST00000315285.9:c.1443T>C MANE Select	ENSP00000320885.3:p.Leu481=
ENST00000621856.2:c.1440T>C	ENSP00000482496.2:p.Leu480=
ENST00000642281.1:c.1180T>C
ENST00000642455.1:c.1344T>C	ENSP00000493827.1:p.Leu448=
ENST00000642751.1:c.1217T>C
ENST00000642999.1:c.1185T>C	ENSP00000496589.1:p.Leu395=
ENST00000643327.1:c.510T>C
ENST00000643334.1:c.1023T>C
ENST00000644408.1:c.1319T>C
ENST00000644954.1:c.1089T>C	ENSP00000494312.1:p.Leu363=
ENST00000645159.1:n.2180T>C
ENST00000645671.1:c.893T>C
ENST00000645730.1:c.622T>C
ENST00000646082.1:c.1089T>C
ENST00000646571.1:c.1347T>C	ENSP00000495015.1:p.Leu449=
ENST00000647007.1:n.1135T>C
ENST00000647133.1:c.943T>C
ENST00000315285.7:c.1443T>C	ENSP00000320885.3:p.Leu481=
ENST00000345662.5:c.1347T>C	ENSP00000340817.1:p.Leu449=
ENST00000615843.4:c.1443T>C	ENSP00000480893.1:p.Leu481=
ENST00000621856.1:c.1185T>C	ENSP00000482496.1:p.Leu395=
NM_014946.3:c.1443T>C , LRG_714t1:c.1443T>C	NP_055761.2:p.Leu481=
NM_199436.1:c.1347T>C	NP_955468.1:p.Leu449=
XM_005264516.3:c.1440T>C	XP_005264573.1:p.Leu480=
XM_011533067.1:c.1443T>C	XP_011531369.1:p.Leu481=
NM_001363823.1:c.1440T>C	NP_001350752.1:p.Leu480=
NM_001363875.1:c.1344T>C	NP_001350804.1:p.Leu448=
XM_005264516.5:c.1440T>C	XP_005264573.1:p.Leu480=
XM_011533067.2:c.1443T>C	XP_011531369.1:p.Leu481=
XM_017004778.2:c.1347T>C	XP_016860267.1:p.Leu449=
NM_001363823.2:c.1440T>C	NP_001350752.1:p.Leu480=
NM_001363875.2:c.1344T>C	NP_001350804.1:p.Leu448=
NM_001377959.1:c.1347T>C	NP_001364888.1:p.Leu449=
NM_014946.4:c.1443T>C MANE Select	NP_055761.2:p.Leu481=
NM_199436.2:c.1347T>C	NP_955468.1:p.Leu449=