Canonical Allele Identifier: CA2333926014

Gene: SYNE4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36006725_36006727delinsTGG , CM000681.2:g.36006725_36006727delinsTGG	GRCh38
NC_000019.9:g.36497627_36497629delinsTGG , CM000681.1:g.36497627_36497629delinsTGG	GRCh37
NC_000019.8:g.41189467_41189469delinsTGG	NCBI36
NG_042831.1:g.7067_7069delinsCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324444.9:c.618+23_618+25delinsCCA MANE Select	ENSP00000316130.3:n.618+23_618+25delinsCCA
ENST00000397428.8:c.67-1290_67-1288delinsCCA
ENST00000465425.2:n.730+23_730+25delinsCCA
ENST00000324444.7:c.618+23_618+25delinsCCA	ENSP00000316130.3:n.618+23_618+25delinsCCA
ENST00000340477.9:c.280-56_280-54delinsCCA	ENSP00000343152.5:n.280-56_280-54delinsCCA
ENST00000397428.7:c.40-1290_40-1288delinsCCA	ENSP00000380572.3:n.40-1290_40-1288delinsCCA
ENST00000465425.1:n.730+23_730+25delinsCCA
ENST00000490730.1:c.618+23_618+25delinsCCA	ENSP00000422716.1:n.618+23_618+25delinsCCA
ENST00000503121.5:c.242+1490_242+1492delinsCCA
ENST00000505054.2:n.395-1290_395-1288delinsCCA
NM_001039876.1:c.618+23_618+25delinsCCA	NP_001034965.1:n.618+23_618+25delinsCCA
NM_001039876.2:c.618+23_618+25delinsCCA	NP_001034965.1:n.618+23_618+25delinsCCA
NM_001297735.1:c.280-56_280-54delinsCCA	NP_001284664.1:n.280-56_280-54delinsCCA
NM_001297735.2:c.280-56_280-54delinsCCA	NP_001284664.1:n.280-56_280-54delinsCCA
XM_005258598.2:c.618+23_618+25delinsCCA	XP_005258655.1:n.618+23_618+25delinsCCA
XM_005258601.2:c.618+23_618+25delinsCCA	XP_005258658.1:n.618+23_618+25delinsCCA
XM_005258604.3:c.618+23_618+25delinsCCA	XP_005258661.1:n.618+23_618+25delinsCCA
NM_001039876.3:c.618+23_618+25delinsCCA MANE Select	NP_001034965.1:n.618+23_618+25delinsCCA
NM_001297735.3:c.280-56_280-54delinsCCA	NP_001284664.1:n.280-56_280-54delinsCCA