Canonical Allele Identifier: CA405432954

Gene: SYNE4

Linked Data

• MyVariant Identifiers: chr19:g.36497570A>T (hg19) ; chr19:g.36006668A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36006668A>T , CM000681.2:g.36006668A>T	GRCh38
NC_000019.9:g.36497570A>T , CM000681.1:g.36497570A>T	GRCh37
NC_000019.8:g.41189410A>T	NCBI36
NG_042831.1:g.7126T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324444.9:c.622T>A MANE Select	ENSP00000316130.3:p.Phe208Ile
ENST00000397428.8:c.67-1231T>A
ENST00000465425.2:n.734T>A
ENST00000324444.7:c.622T>A	ENSP00000316130.3:p.Phe208Ile
ENST00000340477.9:c.283T>A	ENSP00000343152.5:p.Phe95Ile
ENST00000397428.7:c.40-1231T>A	ENSP00000380572.3:n.40-1231T>A
ENST00000465425.1:n.734T>A
ENST00000490730.1:c.622T>A	ENSP00000422716.1:p.Phe208Ile
ENST00000503121.5:c.242+1549T>A
ENST00000505054.2:n.395-1231T>A
NM_001039876.1:c.622T>A	NP_001034965.1:p.Phe208Ile
NM_001039876.2:c.622T>A	NP_001034965.1:p.Phe208Ile
NM_001297735.1:c.283T>A	NP_001284664.1:p.Phe95Ile
NM_001297735.2:c.283T>A	NP_001284664.1:p.Phe95Ile
XM_005258598.2:c.622T>A	XP_005258655.1:p.Phe208Ile
XM_005258601.2:c.618+82T>A	XP_005258658.1:n.618+82T>A
XM_005258604.3:c.622T>A	XP_005258661.1:p.Phe208Ile
NM_001039876.3:c.622T>A MANE Select	NP_001034965.1:p.Phe208Ile
NM_001297735.3:c.283T>A	NP_001284664.1:p.Phe95Ile