Canonical Allele Identifier: CA401188354

Gene: METTL23

Linked Data

• MyVariant Identifiers: chr17:g.74729456G>T (hg19) ; chr17:g.76733374G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76733374G>T , CM000679.2:g.76733374G>T	GRCh38
NC_000017.10:g.74729456G>T , CM000679.1:g.74729456G>T	GRCh37
NC_000017.9:g.72241051G>T	NCBI36
NG_032905.1:g.9038C>A , LRG_640:g.9038C>A
NG_041790.1:g.11545G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000341249.11:c.404G>T MANE Select	ENSP00000341543.5:p.Arg135Met
ENST00000341249.10:c.404G>T	ENSP00000341543.5:p.Arg135Met
ENST00000586200.1:c.47G>T	ENSP00000465959.1:p.Arg16Met
ENST00000586738.5:c.404G>T	ENSP00000468386.1:p.Arg135Met
ENST00000586752.5:c.203G>T	ENSP00000466203.1:p.Arg68Met
ENST00000587459.1:c.238+159G>T	ENSP00000466829.1:n.238+159G>T
ENST00000588302.5:c.203G>T	ENSP00000468704.1:p.Arg68Met
ENST00000588563.5:c.404G>T	ENSP00000467503.1:p.Arg135Met
ENST00000588783.5:c.404G>T	ENSP00000466938.1:p.Arg135Met
ENST00000588822.1:c.203G>T	ENSP00000465430.1:p.Arg68Met
ENST00000589581.1:n.500G>T
ENST00000589977.5:c.404G>T	ENSP00000464965.1:p.Arg135Met
ENST00000590964.5:c.203G>T	ENSP00000465890.1:p.Arg68Met
ENST00000591571.5:c.203G>T	ENSP00000466614.1:p.Arg68Met
ENST00000592849.5:c.404G>T	ENSP00000467527.1:p.Arg135Met
ENST00000615984.4:c.404G>T	ENSP00000482599.1:p.Arg135Met
NM_001080510.4:c.404G>T	NP_001073979.3:p.Arg135Met
NM_001206983.2:c.404G>T	NP_001193912.1:p.Arg135Met
NM_001206984.2:c.404G>T	NP_001193913.1:p.Arg135Met
NM_001206985.2:c.203G>T	NP_001193914.1:p.Arg68Met
NM_001206986.2:c.203G>T	NP_001193915.1:p.Arg68Met
NM_001206987.2:c.203G>T	NP_001193916.1:p.Arg68Met
NM_001302703.1:c.404G>T	NP_001289632.1:p.Arg135Met
NM_001302704.1:c.203G>T	NP_001289633.1:p.Arg68Met
NM_001302705.1:c.392G>T	NP_001289634.1:p.Arg131Met
NR_038193.2:n.431G>T
XM_006721673.2:c.440G>T	XP_006721736.1:p.Arg147Met
XM_006721674.2:c.404G>T	XP_006721737.1:p.Arg135Met
XM_006721675.1:c.392G>T	XP_006721738.1:p.Arg131Met
XM_006721676.2:c.392G>T	XP_006721739.1:p.Arg131Met
XM_006721678.2:c.392G>T	XP_006721741.1:p.Arg131Met
XM_006721679.2:c.371G>T	XP_006721742.1:p.Arg124Met
XM_006721680.2:c.203G>T	XP_006721743.1:p.Arg68Met
XM_011524282.1:c.392G>T	XP_011522584.1:p.Arg131Met
XM_006721674.3:c.404G>T	XP_006721737.1:p.Arg135Met
XM_006721676.3:c.392G>T	XP_006721739.1:p.Arg131Met
XM_006721678.4:c.392G>T	XP_006721741.1:p.Arg131Met
XM_006721679.3:c.371G>T	XP_006721742.1:p.Arg124Met
XM_017024145.2:c.392G>T	XP_016879634.1:p.Arg131Met
XM_017024146.1:c.476G>T	XP_016879635.1:p.Arg159Met
XM_024450563.1:c.*121G>T	XP_024306331.1:n.*121G>T
NM_001080510.5:c.404G>T MANE Select	NP_001073979.3:p.Arg135Met
NM_001206983.3:c.404G>T	NP_001193912.1:p.Arg135Met
NM_001206984.3:c.404G>T	NP_001193913.1:p.Arg135Met
NM_001206985.3:c.203G>T	NP_001193914.1:p.Arg68Met
NM_001206986.3:c.203G>T	NP_001193915.1:p.Arg68Met
NM_001206987.3:c.203G>T	NP_001193916.1:p.Arg68Met
NM_001302703.2:c.404G>T	NP_001289632.1:p.Arg135Met
NM_001302704.2:c.203G>T	NP_001289633.1:p.Arg68Met
NM_001302705.2:c.392G>T	NP_001289634.1:p.Arg131Met
NM_001378348.1:c.404G>T	NP_001365277.1:p.Arg135Met
NM_001378349.1:c.404G>T	NP_001365278.1:p.Arg135Met
NM_001378350.1:c.392G>T	NP_001365279.1:p.Arg131Met
NM_001378351.1:c.392G>T	NP_001365280.1:p.Arg131Met
NM_001378352.1:c.392G>T	NP_001365281.1:p.Arg131Met
NM_001378353.1:c.392G>T	NP_001365282.1:p.Arg131Met
NM_001378354.1:c.203G>T	NP_001365283.1:p.Arg68Met