Canonical Allele Identifier: CA507317027

Gene: SYNE4

Linked Data

• MyVariant Identifiers: chr19:g.36497370C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36006468C>T , CM000681.2:g.36006468C>T	GRCh38
NC_000019.9:g.36497370C>T , CM000681.1:g.36497370C>T	GRCh37
NC_000019.8:g.41189210C>T	NCBI36
NG_042831.1:g.7326G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324444.9:c.822G>A MANE Select	ENSP00000316130.3:p.Glu274=
ENST00000397428.8:c.67-1031G>A
ENST00000465425.2:n.934G>A
ENST00000324444.7:c.822G>A	ENSP00000316130.3:p.Glu274=
ENST00000340477.9:c.483G>A	ENSP00000343152.5:p.Glu161=
ENST00000397428.7:c.40-1031G>A	ENSP00000380572.3:n.40-1031G>A
ENST00000465425.1:n.934G>A
ENST00000490730.1:c.688+134G>A	ENSP00000422716.1:n.688+134G>A
ENST00000503121.5:c.242+1749G>A
ENST00000505054.2:n.395-1031G>A
NM_001039876.1:c.822G>A	NP_001034965.1:p.Glu274=
NM_001039876.2:c.822G>A	NP_001034965.1:p.Glu274=
NM_001297735.1:c.483G>A	NP_001284664.1:p.Glu161=
NM_001297735.2:c.483G>A	NP_001284664.1:p.Glu161=
XM_005258598.2:c.688+134G>A	XP_005258655.1:n.688+134G>A
XM_005258601.2:c.618+282G>A	XP_005258658.1:n.618+282G>A
XM_005258604.3:c.688+134G>A	XP_005258661.1:n.688+134G>A
NM_001039876.3:c.822G>A MANE Select	NP_001034965.1:p.Glu274=
NM_001297735.3:c.483G>A	NP_001284664.1:p.Glu161=