Canonical Allele Identifier: CA425447544

Gene: SPAST

Linked Data

• MyVariant Identifiers: chr2:g.32361634G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32136565G>C , CM000664.2:g.32136565G>C	GRCh38
NC_000002.11:g.32361634G>C , CM000664.1:g.32361634G>C	GRCh37
NC_000002.10:g.32215138G>C	NCBI36
NG_008730.1:g.77955G>C , LRG_714:g.77955G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*908G>C	ENSP00000515816.1:n.*908G>C
ENST00000315285.9:c.1248G>C MANE Select	ENSP00000320885.3:p.Val416=
ENST00000621856.2:c.1245G>C	ENSP00000482496.2:p.Val415=
ENST00000642281.1:c.985G>C
ENST00000642455.1:c.1149G>C	ENSP00000493827.1:p.Val383=
ENST00000642751.1:c.1022G>C
ENST00000642999.1:c.990G>C	ENSP00000496589.1:p.Val330=
ENST00000643327.1:c.407G>C
ENST00000643334.1:c.828G>C
ENST00000644408.1:c.1124G>C
ENST00000644954.1:c.894G>C	ENSP00000494312.1:p.Val298=
ENST00000645159.1:n.1985G>C
ENST00000645671.1:c.698G>C
ENST00000645730.1:c.593-544G>C
ENST00000646082.1:c.894G>C
ENST00000646571.1:c.1152G>C	ENSP00000495015.1:p.Val384=
ENST00000647007.1:n.940G>C
ENST00000647133.1:c.748G>C
ENST00000315285.7:c.1248G>C	ENSP00000320885.3:p.Val416=
ENST00000345662.5:c.1152G>C	ENSP00000340817.1:p.Val384=
ENST00000615843.4:c.1248G>C	ENSP00000480893.1:p.Val416=
ENST00000621856.1:c.990G>C	ENSP00000482496.1:p.Val330=
NM_014946.3:c.1248G>C , LRG_714t1:c.1248G>C	NP_055761.2:p.Val416=
NM_199436.1:c.1152G>C	NP_955468.1:p.Val384=
XM_005264516.3:c.1245G>C	XP_005264573.1:p.Val415=
XM_011533067.1:c.1248G>C	XP_011531369.1:p.Val416=
NM_001363823.1:c.1245G>C	NP_001350752.1:p.Val415=
NM_001363875.1:c.1149G>C	NP_001350804.1:p.Val383=
XM_005264516.5:c.1245G>C	XP_005264573.1:p.Val415=
XM_011533067.2:c.1248G>C	XP_011531369.1:p.Val416=
XM_017004778.2:c.1152G>C	XP_016860267.1:p.Val384=
NM_001363823.2:c.1245G>C	NP_001350752.1:p.Val415=
NM_001363875.2:c.1149G>C	NP_001350804.1:p.Val383=
NM_001377959.1:c.1152G>C	NP_001364888.1:p.Val384=
NM_014946.4:c.1248G>C MANE Select	NP_055761.2:p.Val416=
NM_199436.2:c.1152G>C	NP_955468.1:p.Val384=