Canonical Allele Identifier: CA767798717

Gene: SPAST

Linked Data

• dbSNP Id: rs397984237
• gnomAD v3: 2-32146851-C-CAAAA
• gnomAD v4: 2-32146851-C-CAAAA
• MyVariant Identifiers: chr2:g.32371920_32371921insAAAA (hg19) ; chr2:g.32146851_32146852insAAAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32146877_32146880dup , CM000664.2:g.32146877_32146880dup	GRCh38
NC_000002.11:g.32371946_32371949dup , CM000664.1:g.32371946_32371949dup	GRCh37
NC_000002.10:g.32225450_32225453dup	NCBI36
NG_008730.1:g.88267_88270dup , LRG_714:g.88267_88270dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*1348-341_*1348-338dup	ENSP00000515816.1:n.*1348-341_*1348-338dup
ENST00000315285.9:c.1688-341_1688-338dup MANE Select	ENSP00000320885.3:n.1688-341_1688-338dup
ENST00000621856.2:c.1685-341_1685-338dup	ENSP00000482496.2:n.1685-341_1685-338dup
ENST00000642281.1:c.1425-341_1425-338dup
ENST00000642455.1:c.1589-341_1589-338dup	ENSP00000493827.1:n.1589-341_1589-338dup
ENST00000642751.1:c.1391-341_1391-338dup
ENST00000642999.1:c.1430-341_1430-338dup	ENSP00000496589.1:n.1430-341_1430-338dup
ENST00000643334.1:c.1268-341_1268-338dup
ENST00000644408.1:c.1564-318_1564-315dup
ENST00000644954.1:c.1334-341_1334-338dup	ENSP00000494312.1:n.1334-341_1334-338dup
ENST00000645159.1:n.2425-341_2425-338dup
ENST00000645671.1:c.1067-341_1067-338dup
ENST00000645730.1:c.867-341_867-338dup
ENST00000646082.1:c.1334-341_1334-338dup
ENST00000646571.1:c.1592-341_1592-338dup	ENSP00000495015.1:n.1592-341_1592-338dup
ENST00000647007.1:n.1380-341_1380-338dup
ENST00000647133.1:c.1188-341_1188-338dup
ENST00000315285.7:c.1688-341_1688-338dup	ENSP00000320885.3:n.1688-341_1688-338dup
ENST00000345662.5:c.1592-341_1592-338dup	ENSP00000340817.1:n.1592-341_1592-338dup
ENST00000615843.4:c.1688-341_1688-338dup	ENSP00000480893.1:n.1688-341_1688-338dup
ENST00000621856.1:c.1430-341_1430-338dup	ENSP00000482496.1:n.1430-341_1430-338dup
NM_014946.3:c.1688-341_1688-338dup , LRG_714t1:c.1688-341_1688-338dup	NP_055761.2:n.1688-341_1688-338dup
NM_199436.1:c.1592-341_1592-338dup	NP_955468.1:n.1592-341_1592-338dup
XM_005264516.3:c.1685-341_1685-338dup	XP_005264573.1:n.1685-341_1685-338dup
XM_011533067.1:c.1617-341_1617-338dup	XP_011531369.1:n.1617-341_1617-338dup
NM_001363823.1:c.1685-341_1685-338dup	NP_001350752.1:n.1685-341_1685-338dup
NM_001363875.1:c.1589-341_1589-338dup	NP_001350804.1:n.1589-341_1589-338dup
XM_005264516.5:c.1685-341_1685-338dup	XP_005264573.1:n.1685-341_1685-338dup
XM_011533067.2:c.1617-341_1617-338dup	XP_011531369.1:n.1617-341_1617-338dup
XM_017004778.2:c.1521-341_1521-338dup	XP_016860267.1:n.1521-341_1521-338dup
NM_001363823.2:c.1685-341_1685-338dup	NP_001350752.1:n.1685-341_1685-338dup
NM_001363875.2:c.1589-341_1589-338dup	NP_001350804.1:n.1589-341_1589-338dup
NM_001377959.1:c.1521-341_1521-338dup	NP_001364888.1:n.1521-341_1521-338dup
NM_014946.4:c.1688-341_1688-338dup MANE Select	NP_055761.2:n.1688-341_1688-338dup
NM_199436.2:c.1592-341_1592-338dup	NP_955468.1:n.1592-341_1592-338dup