Canonical Allele Identifier: CA2576760909

Gene: SYNE4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36006423del , CM000681.2:g.36006423del	GRCh38
NC_000019.9:g.36497325del , CM000681.1:g.36497325del	GRCh37
NC_000019.8:g.41189165del	NCBI36
NG_042831.1:g.7372del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324444.9:c.867+1del
ENST00000397428.8:c.67-985del
ENST00000465425.2:n.980del
ENST00000324444.7:c.867+1del
ENST00000340477.9:c.528+1del
ENST00000397428.7:c.40-985del	ENSP00000380572.3:n.40-985del
ENST00000465425.1:n.980del
ENST00000490730.1:c.688+180del	ENSP00000422716.1:n.688+180del
ENST00000503121.5:c.242+1795del
ENST00000505054.2:n.395-985del
NM_001039876.1:c.867+1del
NM_001039876.2:c.867+1del
NM_001297735.1:c.528+1del
NM_001297735.2:c.528+1del
XM_005258598.2:c.688+180del	XP_005258655.1:n.688+180del
XM_005258601.2:c.618+328del	XP_005258658.1:n.618+328del
XM_005258604.3:c.688+180del	XP_005258661.1:n.688+180del
NM_001039876.3:c.867+1del
NM_001297735.3:c.528+1del