Canonical Allele Identifier: CA2333926065

Gene: SYNE4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36006815C= , CM000681.2:g.36006815C=	GRCh38
NC_000019.9:g.36497717C= , CM000681.1:g.36497717C=	GRCh37
NC_000019.8:g.41189557C=	NCBI36
NG_042831.1:g.6979G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324444.9:c.553G= MANE Select	ENSP00000316130.3:p.Ala185=
ENST00000397428.8:c.67-1378G=
ENST00000465425.2:n.665G=
ENST00000324444.7:c.553G=	ENSP00000316130.3:p.Ala185=
ENST00000340477.9:c.280-144G=	ENSP00000343152.5:n.280-144G=
ENST00000397428.7:c.40-1378G=	ENSP00000380572.3:n.40-1378G=
ENST00000465425.1:n.665G=
ENST00000490730.1:c.553G=	ENSP00000422716.1:p.Ala185=
ENST00000503121.5:c.242+1402G=
ENST00000505054.2:n.395-1378G=
NM_001039876.1:c.553G=	NP_001034965.1:p.Ala185=
NM_001039876.2:c.553G=	NP_001034965.1:p.Ala185=
NM_001297735.1:c.280-144G=	NP_001284664.1:n.280-144G=
NM_001297735.2:c.280-144G=	NP_001284664.1:n.280-144G=
XM_005258598.2:c.553G=	XP_005258655.1:p.Ala185=
XM_005258601.2:c.553G=	XP_005258658.1:p.Ala185=
XM_005258604.3:c.553G=	XP_005258661.1:p.Ala185=
NM_001039876.3:c.553G= MANE Select	NP_001034965.1:p.Ala185=
NM_001297735.3:c.280-144G=	NP_001284664.1:n.280-144G=