Canonical Allele Identifier: CA401671630

Gene: METTL4

Linked Data

• MyVariant Identifiers: chr18:g.2547406T>A (hg19) ; chr18:g.2547407T>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000574538.2:c.1022A>T MANE Select	ENSP00000458290.1:p.Glu341Val
ENST00000319888.10:c.1022A>T	ENSP00000320349.6:p.Glu341Val
ENST00000573134.1:n.3323A>T
ENST00000574538.1:c.1022A>T	ENSP00000458290.1:p.Glu341Val
ENST00000576251.5:c.217A>T
NM_001308401.1:c.1022A>T	NP_001295330.1:p.Glu341Val
NM_022840.3:c.1022A>T	NP_073751.3:p.Glu341Val
NM_022840.4:c.1022A>T	NP_073751.3:p.Glu341Val
XM_005258132.2:c.1022A>T	XP_005258189.1:p.Glu341Val
XM_005258133.1:c.581A>T	XP_005258190.1:p.Glu194Val
XM_011525730.1:c.899+5288A>T	XP_011524032.1:n.899+5288A>T
XR_243813.2:n.1545A>T
XM_005258132.4:c.1022A>T	XP_005258189.1:p.Glu341Val
XM_005258133.3:c.581A>T	XP_005258190.1:p.Glu194Val
XM_011525730.3:c.899+5288A>T	XP_011524032.1:n.899+5288A>T
XR_001753260.2:n.1045A>T
XR_243813.4:n.1736A>T
NM_022840.5:c.1022A>T MANE Select	NP_073751.3:p.Glu341Val
NM_001308401.2:c.1022A>T	NP_001295330.1:p.Glu341Val