Canonical Allele Identifier: CA401671627

Gene: METTL4

Linked Data

• MyVariant Identifiers: chr18:g.2547404G>A (hg19) ; chr18:g.2547405G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.2547405G>A , CM000680.2:g.2547405G>A	GRCh38
NC_000018.9:g.2547404G>A , CM000680.1:g.2547404G>A	GRCh37
NC_000018.8:g.2537404G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000574538.2:c.1024C>T MANE Select	ENSP00000458290.1:p.Leu342Phe
ENST00000319888.10:c.1024C>T	ENSP00000320349.6:p.Leu342Phe
ENST00000573134.1:n.3325C>T
ENST00000574538.1:c.1024C>T	ENSP00000458290.1:p.Leu342Phe
ENST00000576251.5:c.219C>T
NM_001308401.1:c.1024C>T	NP_001295330.1:p.Leu342Phe
NM_022840.3:c.1024C>T	NP_073751.3:p.Leu342Phe
NM_022840.4:c.1024C>T	NP_073751.3:p.Leu342Phe
XM_005258132.2:c.1024C>T	XP_005258189.1:p.Leu342Phe
XM_005258133.1:c.583C>T	XP_005258190.1:p.Leu195Phe
XM_011525730.1:c.899+5290C>T	XP_011524032.1:n.899+5290C>T
XR_243813.2:n.1547C>T
XM_005258132.4:c.1024C>T	XP_005258189.1:p.Leu342Phe
XM_005258133.3:c.583C>T	XP_005258190.1:p.Leu195Phe
XM_011525730.3:c.899+5290C>T	XP_011524032.1:n.899+5290C>T
XR_001753260.2:n.1047C>T
XR_243813.4:n.1738C>T
NM_022840.5:c.1024C>T MANE Select	NP_073751.3:p.Leu342Phe
NM_001308401.2:c.1024C>T	NP_001295330.1:p.Leu342Phe