Canonical Allele Identifier: CA401671644
Gene: METTL4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.2547412C>G , CM000680.2:g.2547412C>G GRCh38
NC_000018.9:g.2547411C>G , CM000680.1:g.2547411C>G GRCh37
NC_000018.8:g.2537411C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000574538.2:c.1017G>C MANE Select ENSP00000458290.1:p.Lys339Asn
ENST00000319888.10:c.1017G>C ENSP00000320349.6:p.Lys339Asn
ENST00000573134.1:n.3318G>C
ENST00000574538.1:c.1017G>C ENSP00000458290.1:p.Lys339Asn
ENST00000576251.5:c.212G>C
NM_001308401.1:c.1017G>C NP_001295330.1:p.Lys339Asn
NM_022840.3:c.1017G>C NP_073751.3:p.Lys339Asn
NM_022840.4:c.1017G>C NP_073751.3:p.Lys339Asn
XM_005258132.2:c.1017G>C XP_005258189.1:p.Lys339Asn
XM_005258133.1:c.576G>C XP_005258190.1:p.Lys192Asn
XM_011525730.1:c.899+5283G>C XP_011524032.1:n.899+5283G>C
XR_243813.2:n.1540G>C
XM_005258132.4:c.1017G>C XP_005258189.1:p.Lys339Asn
XM_005258133.3:c.576G>C XP_005258190.1:p.Lys192Asn
XM_011525730.3:c.899+5283G>C XP_011524032.1:n.899+5283G>C
XR_001753260.2:n.1040G>C
XR_243813.4:n.1731G>C
NM_022840.5:c.1017G>C MANE Select NP_073751.3:p.Lys339Asn
NM_001308401.2:c.1017G>C NP_001295330.1:p.Lys339Asn