Canonical Allele Identifier: CA346501281

Gene: SPAST

Linked Data

• MyVariant Identifiers: chr2:g.32352060T>C (hg19) ; chr2:g.32126991T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32126991T>C , CM000664.2:g.32126991T>C	GRCh38
NC_000002.11:g.32352060T>C , CM000664.1:g.32352060T>C	GRCh37
NC_000002.10:g.32205564T>C	NCBI36
NG_008730.1:g.68381T>C , LRG_714:g.68381T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*802T>C	ENSP00000515816.1:n.*802T>C
ENST00000315285.9:c.1142T>C MANE Select	ENSP00000320885.3:p.Phe381Ser
ENST00000621856.2:c.1139T>C	ENSP00000482496.2:p.Phe380Ser
ENST00000642281.1:c.983-9572T>C
ENST00000642455.1:c.1043T>C	ENSP00000493827.1:p.Phe348Ser
ENST00000642751.1:c.916T>C
ENST00000642999.1:c.884T>C	ENSP00000496589.1:p.Phe295Ser
ENST00000643327.1:c.301T>C
ENST00000643334.1:c.722T>C
ENST00000644408.1:c.1018T>C
ENST00000644954.1:c.788T>C	ENSP00000494312.1:p.Phe263Ser
ENST00000645159.1:n.494T>C
ENST00000645550.1:n.355T>C
ENST00000645671.1:c.592T>C
ENST00000645730.1:c.489T>C
ENST00000646082.1:c.788T>C
ENST00000646571.1:c.1046T>C	ENSP00000495015.1:p.Phe349Ser
ENST00000647007.1:n.834T>C
ENST00000647133.1:c.674-1417T>C
ENST00000315285.7:c.1142T>C	ENSP00000320885.3:p.Phe381Ser
ENST00000345662.5:c.1046T>C	ENSP00000340817.1:p.Phe349Ser
ENST00000615843.4:c.1142T>C	ENSP00000480893.1:p.Phe381Ser
ENST00000621856.1:c.884T>C	ENSP00000482496.1:p.Phe295Ser
NM_014946.3:c.1142T>C , LRG_714t1:c.1142T>C	NP_055761.2:p.Phe381Ser
NM_199436.1:c.1046T>C	NP_955468.1:p.Phe349Ser
XM_005264516.3:c.1139T>C	XP_005264573.1:p.Phe380Ser
XM_011533067.1:c.1142T>C	XP_011531369.1:p.Phe381Ser
NM_001363823.1:c.1139T>C	NP_001350752.1:p.Phe380Ser
NM_001363875.1:c.1043T>C	NP_001350804.1:p.Phe348Ser
XM_005264516.5:c.1139T>C	XP_005264573.1:p.Phe380Ser
XM_011533067.2:c.1142T>C	XP_011531369.1:p.Phe381Ser
XM_017004778.2:c.1046T>C	XP_016860267.1:p.Phe349Ser
NM_001363823.2:c.1139T>C	NP_001350752.1:p.Phe380Ser
NM_001363875.2:c.1043T>C	NP_001350804.1:p.Phe348Ser
NM_001377959.1:c.1046T>C	NP_001364888.1:p.Phe349Ser
NM_014946.4:c.1142T>C MANE Select	NP_055761.2:p.Phe381Ser
NM_199436.2:c.1046T>C	NP_955468.1:p.Phe349Ser