Canonical Allele Identifier: CA405431217

Gene: SYNE4

Linked Data

• gnomAD v4: 19-36006421-A-G
• MyVariant Identifiers: chr19:g.36497323A>G (hg19) ; chr19:g.36006421A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36006421A>G , CM000681.2:g.36006421A>G	GRCh38
NC_000019.9:g.36497323A>G , CM000681.1:g.36497323A>G	GRCh37
NC_000019.8:g.41189163A>G	NCBI36
NG_042831.1:g.7373T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324444.9:c.867+2T>C MANE Select	ENSP00000316130.3:n.867+2T>C
ENST00000397428.8:c.67-984T>C
ENST00000465425.2:n.981T>C
ENST00000324444.7:c.867+2T>C	ENSP00000316130.3:n.867+2T>C
ENST00000340477.9:c.528+2T>C	ENSP00000343152.5:n.528+2T>C
ENST00000397428.7:c.40-984T>C	ENSP00000380572.3:n.40-984T>C
ENST00000465425.1:n.981T>C
ENST00000490730.1:c.688+181T>C	ENSP00000422716.1:n.688+181T>C
ENST00000503121.5:c.242+1796T>C
ENST00000505054.2:n.395-984T>C
NM_001039876.1:c.867+2T>C	NP_001034965.1:n.867+2T>C
NM_001039876.2:c.867+2T>C	NP_001034965.1:n.867+2T>C
NM_001297735.1:c.528+2T>C	NP_001284664.1:n.528+2T>C
NM_001297735.2:c.528+2T>C	NP_001284664.1:n.528+2T>C
XM_005258598.2:c.688+181T>C	XP_005258655.1:n.688+181T>C
XM_005258601.2:c.618+329T>C	XP_005258658.1:n.618+329T>C
XM_005258604.3:c.688+181T>C	XP_005258661.1:n.688+181T>C
NM_001039876.3:c.867+2T>C MANE Select	NP_001034965.1:n.867+2T>C
NM_001297735.3:c.528+2T>C	NP_001284664.1:n.528+2T>C