Canonical Allele Identifier: CA2280611165

Gene: METTL4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.2547401T= , CM000680.2:g.2547401T=	GRCh38
NC_000018.9:g.2547400T= , CM000680.1:g.2547400T=	GRCh37
NC_000018.8:g.2537400T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000574538.2:c.1028A= MANE Select	ENSP00000458290.1:p.Tyr343=
ENST00000319888.10:c.1028A=	ENSP00000320349.6:p.Tyr343=
ENST00000573134.1:n.3329A=
ENST00000574538.1:c.1028A=	ENSP00000458290.1:p.Tyr343=
ENST00000576251.5:c.223A=
NM_001308401.1:c.1028A=	NP_001295330.1:p.Tyr343=
NM_022840.3:c.1028A=	NP_073751.3:p.Tyr343=
NM_022840.4:c.1028A=	NP_073751.3:p.Tyr343=
XM_005258132.2:c.1028A=	XP_005258189.1:p.Tyr343=
XM_005258133.1:c.587A=	XP_005258190.1:p.Tyr196=
XM_011525730.1:c.899+5294A=	XP_011524032.1:n.899+5294A=
XR_243813.2:n.1551A=
XM_005258132.4:c.1028A=	XP_005258189.1:p.Tyr343=
XM_005258133.3:c.587A=	XP_005258190.1:p.Tyr196=
XM_011525730.3:c.899+5294A=	XP_011524032.1:n.899+5294A=
XR_001753260.2:n.1051A=
XR_243813.4:n.1742A=
NM_022840.5:c.1028A= MANE Select	NP_073751.3:p.Tyr343=
NM_001308401.2:c.1028A=	NP_001295330.1:p.Tyr343=