Canonical Allele Identifier: CA2333925983

Gene: SYNE4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36006670_36006671delinsAC , CM000681.2:g.36006670_36006671delinsAC	GRCh38
NC_000019.9:g.36497572_36497573delinsAC , CM000681.1:g.36497572_36497573delinsAC	GRCh37
NC_000019.8:g.41189412_41189413delinsAC	NCBI36
NG_042831.1:g.7123_7124delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324444.9:c.619_620delinsGT MANE Select	ENSP00000316130.3:p.Val207=
ENST00000397428.8:c.67-1234_67-1233delinsGT
ENST00000465425.2:n.731_732delinsGT
ENST00000324444.7:c.619_620delinsGT	ENSP00000316130.3:p.Val207=
ENST00000340477.9:c.280_281delinsGT	ENSP00000343152.5:p.Val94=
ENST00000397428.7:c.40-1234_40-1233delinsGT	ENSP00000380572.3:n.40-1234_40-1233delinsGT
ENST00000465425.1:n.731_732delinsGT
ENST00000490730.1:c.619_620delinsGT	ENSP00000422716.1:p.Val207=
ENST00000503121.5:c.242+1546_242+1547delinsGT
ENST00000505054.2:n.395-1234_395-1233delinsGT
NM_001039876.1:c.619_620delinsGT	NP_001034965.1:p.Val207=
NM_001039876.2:c.619_620delinsGT	NP_001034965.1:p.Val207=
NM_001297735.1:c.280_281delinsGT	NP_001284664.1:p.Val94=
NM_001297735.2:c.280_281delinsGT	NP_001284664.1:p.Val94=
XM_005258598.2:c.619_620delinsGT	XP_005258655.1:p.Val207=
XM_005258601.2:c.618+79_618+80delinsGT	XP_005258658.1:n.618+79_618+80delinsGT
XM_005258604.3:c.619_620delinsGT	XP_005258661.1:p.Val207=
NM_001039876.3:c.619_620delinsGT MANE Select	NP_001034965.1:p.Val207=
NM_001297735.3:c.280_281delinsGT	NP_001284664.1:p.Val94=