Canonical Allele Identifier: CA401671621

Gene: METTL4

Linked Data

• gnomAD v4: 18-2547402-A-T
• MyVariant Identifiers: chr18:g.2547401A>T (hg19) ; chr18:g.2547402A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.2547402A>T , CM000680.2:g.2547402A>T	GRCh38
NC_000018.9:g.2547401A>T , CM000680.1:g.2547401A>T	GRCh37
NC_000018.8:g.2537401A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000574538.2:c.1027T>A MANE Select	ENSP00000458290.1:p.Tyr343Asn
ENST00000319888.10:c.1027T>A	ENSP00000320349.6:p.Tyr343Asn
ENST00000573134.1:n.3328T>A
ENST00000574538.1:c.1027T>A	ENSP00000458290.1:p.Tyr343Asn
ENST00000576251.5:c.222T>A
NM_001308401.1:c.1027T>A	NP_001295330.1:p.Tyr343Asn
NM_022840.3:c.1027T>A	NP_073751.3:p.Tyr343Asn
NM_022840.4:c.1027T>A	NP_073751.3:p.Tyr343Asn
XM_005258132.2:c.1027T>A	XP_005258189.1:p.Tyr343Asn
XM_005258133.1:c.586T>A	XP_005258190.1:p.Tyr196Asn
XM_011525730.1:c.899+5293T>A	XP_011524032.1:n.899+5293T>A
XR_243813.2:n.1550T>A
XM_005258132.4:c.1027T>A	XP_005258189.1:p.Tyr343Asn
XM_005258133.3:c.586T>A	XP_005258190.1:p.Tyr196Asn
XM_011525730.3:c.899+5293T>A	XP_011524032.1:n.899+5293T>A
XR_001753260.2:n.1050T>A
XR_243813.4:n.1741T>A
NM_022840.5:c.1027T>A MANE Select	NP_073751.3:p.Tyr343Asn
NM_001308401.2:c.1027T>A	NP_001295330.1:p.Tyr343Asn