Canonical Allele Identifier: CA2333925962

Gene: SYNE4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36006624_36006625delinsTC , CM000681.2:g.36006624_36006625delinsTC	GRCh38
NC_000019.9:g.36497526_36497527delinsTC , CM000681.1:g.36497526_36497527delinsTC	GRCh37
NC_000019.8:g.41189366_41189367delinsTC	NCBI36
NG_042831.1:g.7169_7170delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324444.9:c.665_666delinsGA MANE Select	ENSP00000316130.3:p.Gly222=
ENST00000397428.8:c.67-1188_67-1187delinsGA
ENST00000465425.2:n.777_778delinsGA
ENST00000324444.7:c.665_666delinsGA	ENSP00000316130.3:p.Gly222=
ENST00000340477.9:c.326_327delinsGA	ENSP00000343152.5:p.Gly109=
ENST00000397428.7:c.40-1188_40-1187delinsGA	ENSP00000380572.3:n.40-1188_40-1187delinsGA
ENST00000465425.1:n.777_778delinsGA
ENST00000490730.1:c.665_666delinsGA	ENSP00000422716.1:p.Gly222=
ENST00000503121.5:c.242+1592_242+1593delinsGA
ENST00000505054.2:n.395-1188_395-1187delinsGA
NM_001039876.1:c.665_666delinsGA	NP_001034965.1:p.Gly222=
NM_001039876.2:c.665_666delinsGA	NP_001034965.1:p.Gly222=
NM_001297735.1:c.326_327delinsGA	NP_001284664.1:p.Gly109=
NM_001297735.2:c.326_327delinsGA	NP_001284664.1:p.Gly109=
XM_005258598.2:c.665_666delinsGA	XP_005258655.1:p.Gly222=
XM_005258601.2:c.618+125_618+126delinsGA	XP_005258658.1:n.618+125_618+126delinsGA
XM_005258604.3:c.665_666delinsGA	XP_005258661.1:p.Gly222=
NM_001039876.3:c.665_666delinsGA MANE Select	NP_001034965.1:p.Gly222=
NM_001297735.3:c.326_327delinsGA	NP_001284664.1:p.Gly109=