Canonical Allele Identifier: CA2584626422

Gene: SYNE4

Linked Data

• gnomAD v4: 19-36006367-GCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36006368_36006369del , CM000681.2:g.36006368_36006369del	GRCh38
NC_000019.9:g.36497270_36497271del , CM000681.1:g.36497270_36497271del	GRCh37
NC_000019.8:g.41189110_41189111del	NCBI36
NG_042831.1:g.7425_7426del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324444.9:c.867+54_867+55del MANE Select	ENSP00000316130.3:n.867+54_867+55del
ENST00000397428.8:c.67-932_67-931del
ENST00000465425.2:n.1033_1034del
ENST00000324444.7:c.867+54_867+55del	ENSP00000316130.3:n.867+54_867+55del
ENST00000340477.9:c.528+54_528+55del	ENSP00000343152.5:n.528+54_528+55del
ENST00000397428.7:c.40-932_40-931del	ENSP00000380572.3:n.40-932_40-931del
ENST00000465425.1:n.1033_1034del
ENST00000490730.1:c.688+233_688+234del	ENSP00000422716.1:n.688+233_688+234del
ENST00000503121.5:c.242+1848_242+1849del
ENST00000505054.2:n.395-932_395-931del
NM_001039876.1:c.867+54_867+55del	NP_001034965.1:n.867+54_867+55del
NM_001039876.2:c.867+54_867+55del	NP_001034965.1:n.867+54_867+55del
NM_001297735.1:c.528+54_528+55del	NP_001284664.1:n.528+54_528+55del
NM_001297735.2:c.528+54_528+55del	NP_001284664.1:n.528+54_528+55del
XM_005258598.2:c.688+233_688+234del	XP_005258655.1:n.688+233_688+234del
XM_005258601.2:c.618+381_618+382del	XP_005258658.1:n.618+381_618+382del
XM_005258604.3:c.688+233_688+234del	XP_005258661.1:n.688+233_688+234del
NM_001039876.3:c.867+54_867+55del MANE Select	NP_001034965.1:n.867+54_867+55del
NM_001297735.3:c.528+54_528+55del	NP_001284664.1:n.528+54_528+55del