Canonical Allele Identifier: CA502655545

Gene: METTL4

Linked Data

• MyVariant Identifiers: chr18:g.2547402A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.2547403A>G , CM000680.2:g.2547403A>G	GRCh38
NC_000018.9:g.2547402A>G , CM000680.1:g.2547402A>G	GRCh37
NC_000018.8:g.2537402A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000574538.2:c.1026T>C MANE Select	ENSP00000458290.1:p.Leu342=
ENST00000319888.10:c.1026T>C	ENSP00000320349.6:p.Leu342=
ENST00000573134.1:n.3327T>C
ENST00000574538.1:c.1026T>C	ENSP00000458290.1:p.Leu342=
ENST00000576251.5:c.221T>C
NM_001308401.1:c.1026T>C	NP_001295330.1:p.Leu342=
NM_022840.3:c.1026T>C	NP_073751.3:p.Leu342=
NM_022840.4:c.1026T>C	NP_073751.3:p.Leu342=
XM_005258132.2:c.1026T>C	XP_005258189.1:p.Leu342=
XM_005258133.1:c.585T>C	XP_005258190.1:p.Leu195=
XM_011525730.1:c.899+5292T>C	XP_011524032.1:n.899+5292T>C
XR_243813.2:n.1549T>C
XM_005258132.4:c.1026T>C	XP_005258189.1:p.Leu342=
XM_005258133.3:c.585T>C	XP_005258190.1:p.Leu195=
XM_011525730.3:c.899+5292T>C	XP_011524032.1:n.899+5292T>C
XR_001753260.2:n.1049T>C
XR_243813.4:n.1740T>C
NM_022840.5:c.1026T>C MANE Select	NP_073751.3:p.Leu342=
NM_001308401.2:c.1026T>C	NP_001295330.1:p.Leu342=