Canonical Allele Identifier: CA2584626443

Gene: SYNE4

Linked Data

• gnomAD v4: 19-36006412-TCTGCTCTCACCTCAAGGCCTTGTCCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36006417_36006442del , CM000681.2:g.36006417_36006442del	GRCh38
NC_000019.9:g.36497319_36497344del , CM000681.1:g.36497319_36497344del	GRCh37
NC_000019.8:g.41189159_41189184del	NCBI36
NG_042831.1:g.7356_7381del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324444.9:c.852_867+10del
ENST00000397428.8:c.67-1001_67-976del
ENST00000465425.2:n.964_989del
ENST00000324444.7:c.852_867+10del
ENST00000340477.9:c.513_528+10del
ENST00000397428.7:c.40-1001_40-976del	ENSP00000380572.3:n.40-1001_40-976del
ENST00000465425.1:n.964_989del
ENST00000490730.1:c.688+164_688+189del	ENSP00000422716.1:n.688+164_688+189del
ENST00000503121.5:c.242+1779_242+1804del
ENST00000505054.2:n.395-1001_395-976del
NM_001039876.1:c.852_867+10del
NM_001039876.2:c.852_867+10del
NM_001297735.1:c.513_528+10del
NM_001297735.2:c.513_528+10del
XM_005258598.2:c.688+164_688+189del	XP_005258655.1:n.688+164_688+189del
XM_005258601.2:c.618+312_618+337del	XP_005258658.1:n.618+312_618+337del
XM_005258604.3:c.688+164_688+189del	XP_005258661.1:n.688+164_688+189del
NM_001039876.3:c.852_867+10del
NM_001297735.3:c.513_528+10del