Canonical Allele Identifier: CA405432763

Gene: SYNE4

Linked Data

• MyVariant Identifiers: chr19:g.36497529C>G (hg19) ; chr19:g.36006627C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36006627C>G , CM000681.2:g.36006627C>G	GRCh38
NC_000019.9:g.36497529C>G , CM000681.1:g.36497529C>G	GRCh37
NC_000019.8:g.41189369C>G	NCBI36
NG_042831.1:g.7167G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324444.9:c.663G>C MANE Select	ENSP00000316130.3:p.Glu221Asp
ENST00000397428.8:c.67-1190G>C
ENST00000465425.2:n.775G>C
ENST00000324444.7:c.663G>C	ENSP00000316130.3:p.Glu221Asp
ENST00000340477.9:c.324G>C	ENSP00000343152.5:p.Glu108Asp
ENST00000397428.7:c.40-1190G>C	ENSP00000380572.3:n.40-1190G>C
ENST00000465425.1:n.775G>C
ENST00000490730.1:c.663G>C	ENSP00000422716.1:p.Glu221Asp
ENST00000503121.5:c.242+1590G>C
ENST00000505054.2:n.395-1190G>C
NM_001039876.1:c.663G>C	NP_001034965.1:p.Glu221Asp
NM_001039876.2:c.663G>C	NP_001034965.1:p.Glu221Asp
NM_001297735.1:c.324G>C	NP_001284664.1:p.Glu108Asp
NM_001297735.2:c.324G>C	NP_001284664.1:p.Glu108Asp
XM_005258598.2:c.663G>C	XP_005258655.1:p.Glu221Asp
XM_005258601.2:c.618+123G>C	XP_005258658.1:n.618+123G>C
XM_005258604.3:c.663G>C	XP_005258661.1:p.Glu221Asp
NM_001039876.3:c.663G>C MANE Select	NP_001034965.1:p.Glu221Asp
NM_001297735.3:c.324G>C	NP_001284664.1:p.Glu108Asp