Canonical Allele Identifier: CA401671642
Gene: METTL4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.2547411C>T , CM000680.2:g.2547411C>T GRCh38
NC_000018.9:g.2547410C>T , CM000680.1:g.2547410C>T GRCh37
NC_000018.8:g.2537410C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000574538.2:c.1018G>A MANE Select ENSP00000458290.1:p.Glu340Lys
ENST00000319888.10:c.1018G>A ENSP00000320349.6:p.Glu340Lys
ENST00000573134.1:n.3319G>A
ENST00000574538.1:c.1018G>A ENSP00000458290.1:p.Glu340Lys
ENST00000576251.5:c.213G>A
NM_001308401.1:c.1018G>A NP_001295330.1:p.Glu340Lys
NM_022840.3:c.1018G>A NP_073751.3:p.Glu340Lys
NM_022840.4:c.1018G>A NP_073751.3:p.Glu340Lys
XM_005258132.2:c.1018G>A XP_005258189.1:p.Glu340Lys
XM_005258133.1:c.577G>A XP_005258190.1:p.Glu193Lys
XM_011525730.1:c.899+5284G>A XP_011524032.1:n.899+5284G>A
XR_243813.2:n.1541G>A
XM_005258132.4:c.1018G>A XP_005258189.1:p.Glu340Lys
XM_005258133.3:c.577G>A XP_005258190.1:p.Glu193Lys
XM_011525730.3:c.899+5284G>A XP_011524032.1:n.899+5284G>A
XR_001753260.2:n.1041G>A
XR_243813.4:n.1732G>A
NM_022840.5:c.1018G>A MANE Select NP_073751.3:p.Glu340Lys
NM_001308401.2:c.1018G>A NP_001295330.1:p.Glu340Lys