Canonical Allele Identifier: CA16604222

Gene: SPAST

Linked Data

• ClinVar Variation Id: 392516
• ClinVar RCV Id: RCV000420305 ; RCV003522978
• dbSNP Id: rs1057524526
• MyVariant Identifiers: chr2:g.32340770G>C (hg19) ; chr2:g.32115701G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32115701G>C , CM000664.2:g.32115701G>C	GRCh38
NC_000002.11:g.32340770G>C , CM000664.1:g.32340770G>C	GRCh37
NC_000002.10:g.32194274G>C	NCBI36
NG_008730.1:g.57091G>C , LRG_714:g.57091G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*531-1G>C	ENSP00000515816.1:n.*531-1G>C
ENST00000315285.9:c.871-1G>C MANE Select	ENSP00000320885.3:n.871-1G>C
ENST00000621856.2:c.868-1G>C	ENSP00000482496.2:n.868-1G>C
ENST00000642281.1:c.755-1G>C
ENST00000642455.1:c.772-1G>C	ENSP00000493827.1:n.772-1G>C
ENST00000642751.1:c.645-1G>C
ENST00000642999.1:c.613-1G>C	ENSP00000496589.1:n.613-1G>C
ENST00000643327.1:c.30-1G>C
ENST00000643334.1:c.451-1G>C
ENST00000644408.1:c.747-1G>C
ENST00000644954.1:c.517-1G>C	ENSP00000494312.1:n.517-1G>C
ENST00000645671.1:c.321-1G>C
ENST00000645730.1:c.218-1G>C
ENST00000646082.1:c.517-1G>C
ENST00000646571.1:c.775-1G>C	ENSP00000495015.1:n.775-1G>C
ENST00000647007.1:n.563-1G>C
ENST00000647133.1:c.446-1G>C
ENST00000315285.7:c.871-1G>C	ENSP00000320885.3:n.871-1G>C
ENST00000345662.5:c.775-1G>C	ENSP00000340817.1:n.775-1G>C
ENST00000615843.4:c.871-1G>C	ENSP00000480893.1:n.871-1G>C
ENST00000621856.1:c.613-1G>C	ENSP00000482496.1:n.613-1G>C
NM_014946.3:c.871-1G>C , LRG_714t1:c.871-1G>C	NP_055761.2:n.871-1G>C
NM_199436.1:c.775-1G>C	NP_955468.1:n.775-1G>C
XM_005264516.3:c.868-1G>C	XP_005264573.1:n.868-1G>C
XM_011533067.1:c.871-1G>C	XP_011531369.1:n.871-1G>C
NM_001363823.1:c.868-1G>C	NP_001350752.1:n.868-1G>C
NM_001363875.1:c.772-1G>C	NP_001350804.1:n.772-1G>C
XM_005264516.5:c.868-1G>C	XP_005264573.1:n.868-1G>C
XM_011533067.2:c.871-1G>C	XP_011531369.1:n.871-1G>C
XM_017004778.2:c.775-1G>C	XP_016860267.1:n.775-1G>C
NM_001363823.2:c.868-1G>C	NP_001350752.1:n.868-1G>C
NM_001363875.2:c.772-1G>C	NP_001350804.1:n.772-1G>C
NM_001377959.1:c.775-1G>C	NP_001364888.1:n.775-1G>C
NM_014946.4:c.871-1G>C MANE Select	NP_055761.2:n.871-1G>C
NM_199436.2:c.775-1G>C	NP_955468.1:n.775-1G>C