Canonical Allele Identifier: CA2333926013

Gene: SYNE4

Linked Data

• dbSNP Id: rs1976864868

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36006725del , CM000681.2:g.36006725del	GRCh38
NC_000019.9:g.36497627del , CM000681.1:g.36497627del	GRCh37
NC_000019.8:g.41189467del	NCBI36
NG_042831.1:g.7069del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324444.9:c.618+25del MANE Select	ENSP00000316130.3:n.618+25del
ENST00000397428.8:c.67-1288del
ENST00000465425.2:n.730+25del
ENST00000324444.7:c.618+25del	ENSP00000316130.3:n.618+25del
ENST00000340477.9:c.280-54del	ENSP00000343152.5:n.280-54del
ENST00000397428.7:c.40-1288del	ENSP00000380572.3:n.40-1288del
ENST00000465425.1:n.730+25del
ENST00000490730.1:c.618+25del	ENSP00000422716.1:n.618+25del
ENST00000503121.5:c.242+1492del
ENST00000505054.2:n.395-1288del
NM_001039876.1:c.618+25del	NP_001034965.1:n.618+25del
NM_001039876.2:c.618+25del	NP_001034965.1:n.618+25del
NM_001297735.1:c.280-54del	NP_001284664.1:n.280-54del
NM_001297735.2:c.280-54del	NP_001284664.1:n.280-54del
XM_005258598.2:c.618+25del	XP_005258655.1:n.618+25del
XM_005258601.2:c.618+25del	XP_005258658.1:n.618+25del
XM_005258604.3:c.618+25del	XP_005258661.1:n.618+25del
NM_001039876.3:c.618+25del MANE Select	NP_001034965.1:n.618+25del
NM_001297735.3:c.280-54del	NP_001284664.1:n.280-54del