Canonical Allele Identifier: CA2333925794

Gene: SYNE4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36006389T= , CM000681.2:g.36006389T=	GRCh38
NC_000019.9:g.36497291T= , CM000681.1:g.36497291T=	GRCh37
NC_000019.8:g.41189131T=	NCBI36
NG_042831.1:g.7405A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324444.9:c.867+34A= MANE Select	ENSP00000316130.3:n.867+34A=
ENST00000397428.8:c.67-952A=
ENST00000465425.2:n.1013A=
ENST00000324444.7:c.867+34A=	ENSP00000316130.3:n.867+34A=
ENST00000340477.9:c.528+34A=	ENSP00000343152.5:n.528+34A=
ENST00000397428.7:c.40-952A=	ENSP00000380572.3:n.40-952A=
ENST00000465425.1:n.1013A=
ENST00000490730.1:c.688+213A=	ENSP00000422716.1:n.688+213A=
ENST00000503121.5:c.242+1828A=
ENST00000505054.2:n.395-952A=
NM_001039876.1:c.867+34A=	NP_001034965.1:n.867+34A=
NM_001039876.2:c.867+34A=	NP_001034965.1:n.867+34A=
NM_001297735.1:c.528+34A=	NP_001284664.1:n.528+34A=
NM_001297735.2:c.528+34A=	NP_001284664.1:n.528+34A=
XM_005258598.2:c.688+213A=	XP_005258655.1:n.688+213A=
XM_005258601.2:c.618+361A=	XP_005258658.1:n.618+361A=
XM_005258604.3:c.688+213A=	XP_005258661.1:n.688+213A=
NM_001039876.3:c.867+34A= MANE Select	NP_001034965.1:n.867+34A=
NM_001297735.3:c.528+34A=	NP_001284664.1:n.528+34A=