Canonical Allele Identifier: CA257565033

Gene: METTL3

Linked Data

• dbSNP Id: rs1263791
• gnomAD v3: 14-21501530-T-A
• gnomAD v4: 14-21501530-T-A
• MyVariant Identifiers: chr14:g.21501530T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21501530T>A , CM000676.2:g.21501530T>A	GRCh38

Transcript Alleles

HGVS	Amino-acid change
ENST00000298717.9:c.899+198A>T MANE Select	ENSP00000298717.3:n.899+198A>T
ENST00000298717.8:c.899+198A>T	ENSP00000298717.3:n.899+198A>T
ENST00000396522.6:n.1684+1643A>T
ENST00000536201.5:n.1214A>T
ENST00000537163.5:c.*223+198A>T	ENSP00000442407.1:n.*223+198A>T
ENST00000539760.5:c.747+198A>T
ENST00000543235.5:c.*43+198A>T	ENSP00000445523.1:n.*43+198A>T
ENST00000544248.1:c.724-401A>T	ENSP00000437692.1:n.724-401A>T
ENST00000544500.5:n.833+198A>T
NM_019852.4:c.899+198A>T	NP_062826.2:n.899+198A>T
XM_006720206.2:c.47+198A>T	XP_006720269.1:n.47+198A>T
XM_011536968.1:c.899+198A>T	XP_011535270.1:n.899+198A>T
XM_011536969.1:c.*1+178A>T	XP_011535271.1:n.*1+178A>T
XM_006720206.4:c.47+198A>T	XP_006720269.1:n.47+198A>T
XM_011536968.2:c.899+198A>T	XP_011535270.1:n.899+198A>T
XR_001750438.2:n.1009+178A>T
XR_001750439.2:n.1007+178A>T
NM_019852.5:c.899+198A>T MANE Select	NP_062826.2:n.899+198A>T