Canonical Allele Identifier: CA401671634
Gene: METTL4 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000574538.2:c.1021G>A MANE Select ENSP00000458290.1:p.Glu341Lys
ENST00000319888.10:c.1021G>A ENSP00000320349.6:p.Glu341Lys
ENST00000573134.1:n.3322G>A
ENST00000574538.1:c.1021G>A ENSP00000458290.1:p.Glu341Lys
ENST00000576251.5:c.216G>A
NM_001308401.1:c.1021G>A NP_001295330.1:p.Glu341Lys
NM_022840.3:c.1021G>A NP_073751.3:p.Glu341Lys
NM_022840.4:c.1021G>A NP_073751.3:p.Glu341Lys
XM_005258132.2:c.1021G>A XP_005258189.1:p.Glu341Lys
XM_005258133.1:c.580G>A XP_005258190.1:p.Glu194Lys
XM_011525730.1:c.899+5287G>A XP_011524032.1:n.899+5287G>A
XR_243813.2:n.1544G>A
XM_005258132.4:c.1021G>A XP_005258189.1:p.Glu341Lys
XM_005258133.3:c.580G>A XP_005258190.1:p.Glu194Lys
XM_011525730.3:c.899+5287G>A XP_011524032.1:n.899+5287G>A
XR_001753260.2:n.1044G>A
XR_243813.4:n.1735G>A
NM_022840.5:c.1021G>A MANE Select NP_073751.3:p.Glu341Lys
NM_001308401.2:c.1021G>A NP_001295330.1:p.Glu341Lys