Canonical Allele Identifier: CA2584626456

Gene: SYNE4

Linked Data

• gnomAD v4: 19-36006685-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36006688_36006689del , CM000681.2:g.36006688_36006689del	GRCh38
NC_000019.9:g.36497590_36497591del , CM000681.1:g.36497590_36497591del	GRCh37
NC_000019.8:g.41189430_41189431del	NCBI36
NG_042831.1:g.7107_7108del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324444.9:c.619-16_619-15del MANE Select	ENSP00000316130.3:n.619-16_619-15del
ENST00000397428.8:c.67-1250_67-1249del
ENST00000465425.2:n.731-16_731-15del
ENST00000324444.7:c.619-16_619-15del	ENSP00000316130.3:n.619-16_619-15del
ENST00000340477.9:c.280-16_280-15del	ENSP00000343152.5:n.280-16_280-15del
ENST00000397428.7:c.40-1250_40-1249del	ENSP00000380572.3:n.40-1250_40-1249del
ENST00000465425.1:n.731-16_731-15del
ENST00000490730.1:c.619-16_619-15del	ENSP00000422716.1:n.619-16_619-15del
ENST00000503121.5:c.242+1530_242+1531del
ENST00000505054.2:n.395-1250_395-1249del
NM_001039876.1:c.619-16_619-15del	NP_001034965.1:n.619-16_619-15del
NM_001039876.2:c.619-16_619-15del	NP_001034965.1:n.619-16_619-15del
NM_001297735.1:c.280-16_280-15del	NP_001284664.1:n.280-16_280-15del
NM_001297735.2:c.280-16_280-15del	NP_001284664.1:n.280-16_280-15del
XM_005258598.2:c.619-16_619-15del	XP_005258655.1:n.619-16_619-15del
XM_005258601.2:c.618+63_618+64del	XP_005258658.1:n.618+63_618+64del
XM_005258604.3:c.619-16_619-15del	XP_005258661.1:n.619-16_619-15del
NM_001039876.3:c.619-16_619-15del MANE Select	NP_001034965.1:n.619-16_619-15del
NM_001297735.3:c.280-16_280-15del	NP_001284664.1:n.280-16_280-15del