Canonical Allele Identifier: CA2333925792

Gene: SYNE4

Linked Data

• dbSNP Id: rs1976850130
• gnomAD v4: 19-36006386-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36006386G>T , CM000681.2:g.36006386G>T	GRCh38
NC_000019.9:g.36497288G>T , CM000681.1:g.36497288G>T	GRCh37
NC_000019.8:g.41189128G>T	NCBI36
NG_042831.1:g.7408C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324444.9:c.867+37C>A MANE Select	ENSP00000316130.3:n.867+37C>A
ENST00000397428.8:c.67-949C>A
ENST00000465425.2:n.1016C>A
ENST00000324444.7:c.867+37C>A	ENSP00000316130.3:n.867+37C>A
ENST00000340477.9:c.528+37C>A	ENSP00000343152.5:n.528+37C>A
ENST00000397428.7:c.40-949C>A	ENSP00000380572.3:n.40-949C>A
ENST00000465425.1:n.1016C>A
ENST00000490730.1:c.688+216C>A	ENSP00000422716.1:n.688+216C>A
ENST00000503121.5:c.242+1831C>A
ENST00000505054.2:n.395-949C>A
NM_001039876.1:c.867+37C>A	NP_001034965.1:n.867+37C>A
NM_001039876.2:c.867+37C>A	NP_001034965.1:n.867+37C>A
NM_001297735.1:c.528+37C>A	NP_001284664.1:n.528+37C>A
NM_001297735.2:c.528+37C>A	NP_001284664.1:n.528+37C>A
XM_005258598.2:c.688+216C>A	XP_005258655.1:n.688+216C>A
XM_005258601.2:c.618+364C>A	XP_005258658.1:n.618+364C>A
XM_005258604.3:c.688+216C>A	XP_005258661.1:n.688+216C>A
NM_001039876.3:c.867+37C>A MANE Select	NP_001034965.1:n.867+37C>A
NM_001297735.3:c.528+37C>A	NP_001284664.1:n.528+37C>A