Canonical Allele Identifier: CA502655560

Gene: METTL4

Linked Data

• MyVariant Identifiers: chr18:g.2547414T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.2547415T>A , CM000680.2:g.2547415T>A	GRCh38
NC_000018.9:g.2547414T>A , CM000680.1:g.2547414T>A	GRCh37
NC_000018.8:g.2537414T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000574538.2:c.1014A>T MANE Select	ENSP00000458290.1:p.Ile338=
ENST00000319888.10:c.1014A>T	ENSP00000320349.6:p.Ile338=
ENST00000573134.1:n.3315A>T
ENST00000574538.1:c.1014A>T	ENSP00000458290.1:p.Ile338=
ENST00000576251.5:c.209A>T
NM_001308401.1:c.1014A>T	NP_001295330.1:p.Ile338=
NM_022840.3:c.1014A>T	NP_073751.3:p.Ile338=
NM_022840.4:c.1014A>T	NP_073751.3:p.Ile338=
XM_005258132.2:c.1014A>T	XP_005258189.1:p.Ile338=
XM_005258133.1:c.573A>T	XP_005258190.1:p.Ile191=
XM_011525730.1:c.899+5280A>T	XP_011524032.1:n.899+5280A>T
XR_243813.2:n.1537A>T
XM_005258132.4:c.1014A>T	XP_005258189.1:p.Ile338=
XM_005258133.3:c.573A>T	XP_005258190.1:p.Ile191=
XM_011525730.3:c.899+5280A>T	XP_011524032.1:n.899+5280A>T
XR_001753260.2:n.1037A>T
XR_243813.4:n.1728A>T
NM_022840.5:c.1014A>T MANE Select	NP_073751.3:p.Ile338=
NM_001308401.2:c.1014A>T	NP_001295330.1:p.Ile338=