Canonical Allele Identifier: CA2280611167

Gene: METTL4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.2547407T= , CM000680.2:g.2547407T=	GRCh38
NC_000018.9:g.2547406T= , CM000680.1:g.2547406T=	GRCh37
NC_000018.8:g.2537406T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000574538.2:c.1022A= MANE Select	ENSP00000458290.1:p.Glu341=
ENST00000319888.10:c.1022A=	ENSP00000320349.6:p.Glu341=
ENST00000573134.1:n.3323A=
ENST00000574538.1:c.1022A=	ENSP00000458290.1:p.Glu341=
ENST00000576251.5:c.217A=
NM_001308401.1:c.1022A=	NP_001295330.1:p.Glu341=
NM_022840.3:c.1022A=	NP_073751.3:p.Glu341=
NM_022840.4:c.1022A=	NP_073751.3:p.Glu341=
XM_005258132.2:c.1022A=	XP_005258189.1:p.Glu341=
XM_005258133.1:c.581A=	XP_005258190.1:p.Glu194=
XM_011525730.1:c.899+5288A=	XP_011524032.1:n.899+5288A=
XR_243813.2:n.1545A=
XM_005258132.4:c.1022A=	XP_005258189.1:p.Glu341=
XM_005258133.3:c.581A=	XP_005258190.1:p.Glu194=
XM_011525730.3:c.899+5288A=	XP_011524032.1:n.899+5288A=
XR_001753260.2:n.1045A=
XR_243813.4:n.1736A=
NM_022840.5:c.1022A= MANE Select	NP_073751.3:p.Glu341=
NM_001308401.2:c.1022A=	NP_001295330.1:p.Glu341=