Canonical Allele Identifier: CA2333925963

Gene: SYNE4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36006626C= , CM000681.2:g.36006626C=	GRCh38
NC_000019.9:g.36497528C= , CM000681.1:g.36497528C=	GRCh37
NC_000019.8:g.41189368C=	NCBI36
NG_042831.1:g.7168G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324444.9:c.664G= MANE Select	ENSP00000316130.3:p.Gly222=
ENST00000397428.8:c.67-1189G=
ENST00000465425.2:n.776G=
ENST00000324444.7:c.664G=	ENSP00000316130.3:p.Gly222=
ENST00000340477.9:c.325G=	ENSP00000343152.5:p.Gly109=
ENST00000397428.7:c.40-1189G=	ENSP00000380572.3:n.40-1189G=
ENST00000465425.1:n.776G=
ENST00000490730.1:c.664G=	ENSP00000422716.1:p.Gly222=
ENST00000503121.5:c.242+1591G=
ENST00000505054.2:n.395-1189G=
NM_001039876.1:c.664G=	NP_001034965.1:p.Gly222=
NM_001039876.2:c.664G=	NP_001034965.1:p.Gly222=
NM_001297735.1:c.325G=	NP_001284664.1:p.Gly109=
NM_001297735.2:c.325G=	NP_001284664.1:p.Gly109=
XM_005258598.2:c.664G=	XP_005258655.1:p.Gly222=
XM_005258601.2:c.618+124G=	XP_005258658.1:n.618+124G=
XM_005258604.3:c.664G=	XP_005258661.1:p.Gly222=
NM_001039876.3:c.664G= MANE Select	NP_001034965.1:p.Gly222=
NM_001297735.3:c.325G=	NP_001284664.1:p.Gly109=