Canonical Allele Identifier: CA2333925976

Gene: SYNE4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36006652G= , CM000681.2:g.36006652G=	GRCh38
NC_000019.9:g.36497554G= , CM000681.1:g.36497554G=	GRCh37
NC_000019.8:g.41189394G=	NCBI36
NG_042831.1:g.7142C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324444.9:c.638C= MANE Select	ENSP00000316130.3:p.Thr213=
ENST00000397428.8:c.67-1215C=
ENST00000465425.2:n.750C=
ENST00000324444.7:c.638C=	ENSP00000316130.3:p.Thr213=
ENST00000340477.9:c.299C=	ENSP00000343152.5:p.Thr100=
ENST00000397428.7:c.40-1215C=	ENSP00000380572.3:n.40-1215C=
ENST00000465425.1:n.750C=
ENST00000490730.1:c.638C=	ENSP00000422716.1:p.Thr213=
ENST00000503121.5:c.242+1565C=
ENST00000505054.2:n.395-1215C=
NM_001039876.1:c.638C=	NP_001034965.1:p.Thr213=
NM_001039876.2:c.638C=	NP_001034965.1:p.Thr213=
NM_001297735.1:c.299C=	NP_001284664.1:p.Thr100=
NM_001297735.2:c.299C=	NP_001284664.1:p.Thr100=
XM_005258598.2:c.638C=	XP_005258655.1:p.Thr213=
XM_005258601.2:c.618+98C=	XP_005258658.1:n.618+98C=
XM_005258604.3:c.638C=	XP_005258661.1:p.Thr213=
NM_001039876.3:c.638C= MANE Select	NP_001034965.1:p.Thr213=
NM_001297735.3:c.299C=	NP_001284664.1:p.Thr100=