Canonical Allele Identifier: CA2280611168

Gene: METTL4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.2547408C= , CM000680.2:g.2547408C=	GRCh38
NC_000018.9:g.2547407C= , CM000680.1:g.2547407C=	GRCh37
NC_000018.8:g.2537407C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000574538.2:c.1021G= MANE Select	ENSP00000458290.1:p.Glu341=
ENST00000319888.10:c.1021G=	ENSP00000320349.6:p.Glu341=
ENST00000573134.1:n.3322G=
ENST00000574538.1:c.1021G=	ENSP00000458290.1:p.Glu341=
ENST00000576251.5:c.216G=
NM_001308401.1:c.1021G=	NP_001295330.1:p.Glu341=
NM_022840.3:c.1021G=	NP_073751.3:p.Glu341=
NM_022840.4:c.1021G=	NP_073751.3:p.Glu341=
XM_005258132.2:c.1021G=	XP_005258189.1:p.Glu341=
XM_005258133.1:c.580G=	XP_005258190.1:p.Glu194=
XM_011525730.1:c.899+5287G=	XP_011524032.1:n.899+5287G=
XR_243813.2:n.1544G=
XM_005258132.4:c.1021G=	XP_005258189.1:p.Glu341=
XM_005258133.3:c.580G=	XP_005258190.1:p.Glu194=
XM_011525730.3:c.899+5287G=	XP_011524032.1:n.899+5287G=
XR_001753260.2:n.1044G=
XR_243813.4:n.1735G=
NM_022840.5:c.1021G= MANE Select	NP_073751.3:p.Glu341=
NM_001308401.2:c.1021G=	NP_001295330.1:p.Glu341=