Canonical Allele Identifier: CA2333925951

Gene: SYNE4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36006600A= , CM000681.2:g.36006600A=	GRCh38
NC_000019.9:g.36497502A= , CM000681.1:g.36497502A=	GRCh37
NC_000019.8:g.41189342A=	NCBI36
NG_042831.1:g.7194T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324444.9:c.690T= MANE Select	ENSP00000316130.3:p.Gly230=
ENST00000397428.8:c.67-1163T=
ENST00000465425.2:n.802T=
ENST00000324444.7:c.690T=	ENSP00000316130.3:p.Gly230=
ENST00000340477.9:c.351T=	ENSP00000343152.5:p.Gly117=
ENST00000397428.7:c.40-1163T=	ENSP00000380572.3:n.40-1163T=
ENST00000465425.1:n.802T=
ENST00000490730.1:c.688+2T=	ENSP00000422716.1:n.688+2T=
ENST00000503121.5:c.242+1617T=
ENST00000505054.2:n.395-1163T=
NM_001039876.1:c.690T=	NP_001034965.1:p.Gly230=
NM_001039876.2:c.690T=	NP_001034965.1:p.Gly230=
NM_001297735.1:c.351T=	NP_001284664.1:p.Gly117=
NM_001297735.2:c.351T=	NP_001284664.1:p.Gly117=
XM_005258598.2:c.688+2T=	XP_005258655.1:n.688+2T=
XM_005258601.2:c.618+150T=	XP_005258658.1:n.618+150T=
XM_005258604.3:c.688+2T=	XP_005258661.1:n.688+2T=
NM_001039876.3:c.690T= MANE Select	NP_001034965.1:p.Gly230=
NM_001297735.3:c.351T=	NP_001284664.1:p.Gly117=