Canonical Allele Identifier: CA401671647
Gene: METTL4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.2547413T>G , CM000680.2:g.2547413T>G GRCh38
NC_000018.9:g.2547412T>G , CM000680.1:g.2547412T>G GRCh37
NC_000018.8:g.2537412T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000574538.2:c.1016A>C MANE Select ENSP00000458290.1:p.Lys339Thr
ENST00000319888.10:c.1016A>C ENSP00000320349.6:p.Lys339Thr
ENST00000573134.1:n.3317A>C
ENST00000574538.1:c.1016A>C ENSP00000458290.1:p.Lys339Thr
ENST00000576251.5:c.211A>C
NM_001308401.1:c.1016A>C NP_001295330.1:p.Lys339Thr
NM_022840.3:c.1016A>C NP_073751.3:p.Lys339Thr
NM_022840.4:c.1016A>C NP_073751.3:p.Lys339Thr
XM_005258132.2:c.1016A>C XP_005258189.1:p.Lys339Thr
XM_005258133.1:c.575A>C XP_005258190.1:p.Lys192Thr
XM_011525730.1:c.899+5282A>C XP_011524032.1:n.899+5282A>C
XR_243813.2:n.1539A>C
XM_005258132.4:c.1016A>C XP_005258189.1:p.Lys339Thr
XM_005258133.3:c.575A>C XP_005258190.1:p.Lys192Thr
XM_011525730.3:c.899+5282A>C XP_011524032.1:n.899+5282A>C
XR_001753260.2:n.1039A>C
XR_243813.4:n.1730A>C
NM_022840.5:c.1016A>C MANE Select NP_073751.3:p.Lys339Thr
NM_001308401.2:c.1016A>C NP_001295330.1:p.Lys339Thr