Canonical Allele Identifier: CA346501372

Gene: SPAST

Linked Data

• MyVariant Identifiers: chr2:g.32353482A>C (hg19) ; chr2:g.32128413A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32128413A>C , CM000664.2:g.32128413A>C	GRCh38
NC_000002.11:g.32353482A>C , CM000664.1:g.32353482A>C	GRCh37
NC_000002.10:g.32206986A>C	NCBI36
NG_008730.1:g.69803A>C , LRG_714:g.69803A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704289.1:c.*839A>C	ENSP00000515816.1:n.*839A>C
ENST00000315285.9:c.1179A>C MANE Select	ENSP00000320885.3:p.Lys393Asn
ENST00000621856.2:c.1176A>C	ENSP00000482496.2:p.Lys392Asn
ENST00000642281.1:c.983-8150A>C
ENST00000642455.1:c.1080A>C	ENSP00000493827.1:p.Lys360Asn
ENST00000642751.1:c.953A>C
ENST00000642999.1:c.921A>C	ENSP00000496589.1:p.Lys307Asn
ENST00000643327.1:c.338A>C
ENST00000643334.1:c.759A>C
ENST00000644408.1:c.1055A>C
ENST00000644954.1:c.825A>C	ENSP00000494312.1:p.Lys275Asn
ENST00000645159.1:n.1916A>C
ENST00000645550.1:n.392A>C
ENST00000645671.1:c.629A>C
ENST00000645730.1:c.526A>C
ENST00000646082.1:c.825A>C
ENST00000646571.1:c.1083A>C	ENSP00000495015.1:p.Lys361Asn
ENST00000647007.1:n.871A>C
ENST00000647133.1:c.679A>C
ENST00000315285.7:c.1179A>C	ENSP00000320885.3:p.Lys393Asn
ENST00000345662.5:c.1083A>C	ENSP00000340817.1:p.Lys361Asn
ENST00000615843.4:c.1179A>C	ENSP00000480893.1:p.Lys393Asn
ENST00000621856.1:c.921A>C	ENSP00000482496.1:p.Lys307Asn
NM_014946.3:c.1179A>C , LRG_714t1:c.1179A>C	NP_055761.2:p.Lys393Asn
NM_199436.1:c.1083A>C	NP_955468.1:p.Lys361Asn
XM_005264516.3:c.1176A>C	XP_005264573.1:p.Lys392Asn
XM_011533067.1:c.1179A>C	XP_011531369.1:p.Lys393Asn
NM_001363823.1:c.1176A>C	NP_001350752.1:p.Lys392Asn
NM_001363875.1:c.1080A>C	NP_001350804.1:p.Lys360Asn
XM_005264516.5:c.1176A>C	XP_005264573.1:p.Lys392Asn
XM_011533067.2:c.1179A>C	XP_011531369.1:p.Lys393Asn
XM_017004778.2:c.1083A>C	XP_016860267.1:p.Lys361Asn
NM_001363823.2:c.1176A>C	NP_001350752.1:p.Lys392Asn
NM_001363875.2:c.1080A>C	NP_001350804.1:p.Lys360Asn
NM_001377959.1:c.1083A>C	NP_001364888.1:p.Lys361Asn
NM_014946.4:c.1179A>C MANE Select	NP_055761.2:p.Lys393Asn
NM_199436.2:c.1083A>C	NP_955468.1:p.Lys361Asn