Canonical Allele Identifier: CA2333925954

Gene: SYNE4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36006605G= , CM000681.2:g.36006605G=	GRCh38
NC_000019.9:g.36497507G= , CM000681.1:g.36497507G=	GRCh37
NC_000019.8:g.41189347G=	NCBI36
NG_042831.1:g.7189C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324444.9:c.685C= MANE Select	ENSP00000316130.3:p.Pro229=
ENST00000397428.8:c.67-1168C=
ENST00000465425.2:n.797C=
ENST00000324444.7:c.685C=	ENSP00000316130.3:p.Pro229=
ENST00000340477.9:c.346C=	ENSP00000343152.5:p.Pro116=
ENST00000397428.7:c.40-1168C=	ENSP00000380572.3:n.40-1168C=
ENST00000465425.1:n.797C=
ENST00000490730.1:c.685C=	ENSP00000422716.1:p.Pro229=
ENST00000503121.5:c.242+1612C=
ENST00000505054.2:n.395-1168C=
NM_001039876.1:c.685C=	NP_001034965.1:p.Pro229=
NM_001039876.2:c.685C=	NP_001034965.1:p.Pro229=
NM_001297735.1:c.346C=	NP_001284664.1:p.Pro116=
NM_001297735.2:c.346C=	NP_001284664.1:p.Pro116=
XM_005258598.2:c.685C=	XP_005258655.1:p.Pro229=
XM_005258601.2:c.618+145C=	XP_005258658.1:n.618+145C=
XM_005258604.3:c.685C=	XP_005258661.1:p.Pro229=
NM_001039876.3:c.685C= MANE Select	NP_001034965.1:p.Pro229=
NM_001297735.3:c.346C=	NP_001284664.1:p.Pro116=