Canonical Allele Identifier: CA405432207

Gene: SYNE4

Linked Data

• gnomAD v4: 19-36006533-C-T
• MyVariant Identifiers: chr19:g.36497435C>T (hg19) ; chr19:g.36006533C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36006533C>T , CM000681.2:g.36006533C>T	GRCh38
NC_000019.9:g.36497435C>T , CM000681.1:g.36497435C>T	GRCh37
NC_000019.8:g.41189275C>T	NCBI36
NG_042831.1:g.7261G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324444.9:c.757G>A MANE Select	ENSP00000316130.3:p.Gly253Arg
ENST00000397428.8:c.67-1096G>A
ENST00000465425.2:n.869G>A
ENST00000324444.7:c.757G>A	ENSP00000316130.3:p.Gly253Arg
ENST00000340477.9:c.418G>A	ENSP00000343152.5:p.Gly140Arg
ENST00000397428.7:c.40-1096G>A	ENSP00000380572.3:n.40-1096G>A
ENST00000465425.1:n.869G>A
ENST00000490730.1:c.688+69G>A	ENSP00000422716.1:n.688+69G>A
ENST00000503121.5:c.242+1684G>A
ENST00000505054.2:n.395-1096G>A
NM_001039876.1:c.757G>A	NP_001034965.1:p.Gly253Arg
NM_001039876.2:c.757G>A	NP_001034965.1:p.Gly253Arg
NM_001297735.1:c.418G>A	NP_001284664.1:p.Gly140Arg
NM_001297735.2:c.418G>A	NP_001284664.1:p.Gly140Arg
XM_005258598.2:c.688+69G>A	XP_005258655.1:n.688+69G>A
XM_005258601.2:c.618+217G>A	XP_005258658.1:n.618+217G>A
XM_005258604.3:c.688+69G>A	XP_005258661.1:n.688+69G>A
NM_001039876.3:c.757G>A MANE Select	NP_001034965.1:p.Gly253Arg
NM_001297735.3:c.418G>A	NP_001284664.1:p.Gly140Arg