Canonical Allele Identifier: CA507317086

Gene: SYNE4

Linked Data

• MyVariant Identifiers: chr19:g.36497415C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36006513C>A , CM000681.2:g.36006513C>A	GRCh38
NC_000019.9:g.36497415C>A , CM000681.1:g.36497415C>A	GRCh37
NC_000019.8:g.41189255C>A	NCBI36
NG_042831.1:g.7281G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324444.9:c.777G>T MANE Select	ENSP00000316130.3:p.Gly259=
ENST00000397428.8:c.67-1076G>T
ENST00000465425.2:n.889G>T
ENST00000324444.7:c.777G>T	ENSP00000316130.3:p.Gly259=
ENST00000340477.9:c.438G>T	ENSP00000343152.5:p.Gly146=
ENST00000397428.7:c.40-1076G>T	ENSP00000380572.3:n.40-1076G>T
ENST00000465425.1:n.889G>T
ENST00000490730.1:c.688+89G>T	ENSP00000422716.1:n.688+89G>T
ENST00000503121.5:c.242+1704G>T
ENST00000505054.2:n.395-1076G>T
NM_001039876.1:c.777G>T	NP_001034965.1:p.Gly259=
NM_001039876.2:c.777G>T	NP_001034965.1:p.Gly259=
NM_001297735.1:c.438G>T	NP_001284664.1:p.Gly146=
NM_001297735.2:c.438G>T	NP_001284664.1:p.Gly146=
XM_005258598.2:c.688+89G>T	XP_005258655.1:n.688+89G>T
XM_005258601.2:c.618+237G>T	XP_005258658.1:n.618+237G>T
XM_005258604.3:c.688+89G>T	XP_005258661.1:n.688+89G>T
NM_001039876.3:c.777G>T MANE Select	NP_001034965.1:p.Gly259=
NM_001297735.3:c.438G>T	NP_001284664.1:p.Gly146=