Canonical Allele Identifier: CA346504343

Gene: SPAST

Linked Data

• dbSNP Id: rs1237484416
• gnomAD v3: 2-32147235-G-A
• gnomAD v4: 2-32147235-G-A
• MyVariant Identifiers: chr2:g.32372304G>A (hg19) ; chr2:g.32147235G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32147235G>A , CM000664.2:g.32147235G>A	GRCh38
NC_000002.11:g.32372304G>A , CM000664.1:g.32372304G>A	GRCh37
NC_000002.10:g.32225808G>A	NCBI36
NG_008730.1:g.88625G>A , LRG_714:g.88625G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*1365G>A	ENSP00000515816.1:n.*1365G>A
ENST00000315285.9:c.1705G>A MANE Select	ENSP00000320885.3:p.Val569Met
ENST00000621856.2:c.1702G>A	ENSP00000482496.2:p.Val568Met
ENST00000642281.1:c.1442G>A
ENST00000642455.1:c.1606G>A	ENSP00000493827.1:p.Val536Met
ENST00000642751.1:c.1408G>A
ENST00000642999.1:c.1447G>A	ENSP00000496589.1:p.Val483Met
ENST00000643334.1:c.1285G>A
ENST00000644408.1:c.1604G>A
ENST00000644954.1:c.1351G>A	ENSP00000494312.1:p.Val451Met
ENST00000645159.1:n.2442G>A
ENST00000645671.1:c.1084G>A
ENST00000645730.1:c.884G>A
ENST00000646082.1:c.1351G>A
ENST00000646571.1:c.1609G>A	ENSP00000495015.1:p.Val537Met
ENST00000647007.1:n.1397G>A
ENST00000647133.1:c.1205G>A
ENST00000315285.7:c.1705G>A	ENSP00000320885.3:p.Val569Met
ENST00000345662.5:c.1609G>A	ENSP00000340817.1:p.Val537Met
ENST00000615843.4:c.1705G>A	ENSP00000480893.1:p.Val569Met
ENST00000621856.1:c.1447G>A	ENSP00000482496.1:p.Val483Met
NM_014946.3:c.1705G>A , LRG_714t1:c.1705G>A	NP_055761.2:p.Val569Met
NM_199436.1:c.1609G>A	NP_955468.1:p.Val537Met
XM_005264516.3:c.1702G>A	XP_005264573.1:p.Val568Met
XM_011533067.1:c.1634G>A	XP_011531369.1:p.Gly545Asp
NM_001363823.1:c.1702G>A	NP_001350752.1:p.Val568Met
NM_001363875.1:c.1606G>A	NP_001350804.1:p.Val536Met
XM_005264516.5:c.1702G>A	XP_005264573.1:p.Val568Met
XM_011533067.2:c.1634G>A	XP_011531369.1:p.Gly545Asp
XM_017004778.2:c.1538G>A	XP_016860267.1:p.Gly513Asp
NM_001363823.2:c.1702G>A	NP_001350752.1:p.Val568Met
NM_001363875.2:c.1606G>A	NP_001350804.1:p.Val536Met
NM_001377959.1:c.1538G>A	NP_001364888.1:p.Gly513Asp
NM_014946.4:c.1705G>A MANE Select	NP_055761.2:p.Val569Met
NM_199436.2:c.1609G>A	NP_955468.1:p.Val537Met