Canonical Allele Identifier: CA2276140566
Gene: METTL23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.76733474A= , CM000679.2:g.76733474A= GRCh38
NC_000017.10:g.74729556A= , CM000679.1:g.74729556A= GRCh37
NC_000017.9:g.72241151A= NCBI36
NG_032905.1:g.8938T= , LRG_640:g.8938T=
NG_041790.1:g.11645A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000341249.11:c.408-47A= MANE Select ENSP00000341543.5:n.408-47A=
ENST00000341249.10:c.408-47A= ENSP00000341543.5:n.408-47A=
ENST00000586200.1:c.51-47A= ENSP00000465959.1:n.51-47A=
ENST00000586738.5:c.412-47A= ENSP00000468386.1:n.412-47A=
ENST00000586752.5:c.207-47A= ENSP00000466203.1:n.207-47A=
ENST00000587459.1:c.238+259A= ENSP00000466829.1:n.238+259A=
ENST00000588302.5:c.211-47A= ENSP00000468704.1:n.211-47A=
ENST00000588563.5:c.408-47A= ENSP00000467503.1:n.408-47A=
ENST00000588783.5:c.412-47A= ENSP00000466938.1:n.412-47A=
ENST00000588822.1:c.207-47A= ENSP00000465430.1:n.207-47A=
ENST00000589581.1:n.504-47A=
ENST00000589977.5:c.*63A= ENSP00000464965.1:n.*63A=
ENST00000590964.5:c.207-47A= ENSP00000465890.1:n.207-47A=
ENST00000591571.5:c.*63A= ENSP00000466614.1:n.*63A=
ENST00000592849.5:c.408-47A= ENSP00000467527.1:n.408-47A=
ENST00000615984.4:c.408-47A= ENSP00000482599.1:n.408-47A=
NM_001080510.4:c.408-47A= NP_001073979.3:n.408-47A=
NM_001206983.2:c.408-47A= NP_001193912.1:n.408-47A=
NM_001206984.2:c.408-47A= NP_001193913.1:n.408-47A=
NM_001206985.2:c.207-47A= NP_001193914.1:n.207-47A=
NM_001206986.2:c.207-47A= NP_001193915.1:n.207-47A=
NM_001206987.2:c.207-47A= NP_001193916.1:n.207-47A=
NM_001302703.1:c.408-47A= NP_001289632.1:n.408-47A=
NM_001302704.1:c.207-47A= NP_001289633.1:n.207-47A=
NM_001302705.1:c.396-47A= NP_001289634.1:n.396-47A=
NR_038193.2:n.435-47A=
XM_006721673.2:c.444-47A= XP_006721736.1:n.444-47A=
XM_006721674.2:c.408-47A= XP_006721737.1:n.408-47A=
XM_006721675.1:c.396-47A= XP_006721738.1:n.396-47A=
XM_006721676.2:c.396-47A= XP_006721739.1:n.396-47A=
XM_006721678.2:c.396-47A= XP_006721741.1:n.396-47A=
XM_006721679.2:c.375-47A= XP_006721742.1:n.375-47A=
XM_006721680.2:c.207-47A= XP_006721743.1:n.207-47A=
XM_011524282.1:c.396-47A= XP_011522584.1:n.396-47A=
XM_006721674.3:c.408-47A= XP_006721737.1:n.408-47A=
XM_006721676.3:c.396-47A= XP_006721739.1:n.396-47A=
XM_006721678.4:c.396-47A= XP_006721741.1:n.396-47A=
XM_006721679.3:c.375-47A= XP_006721742.1:n.375-47A=
XM_017024145.2:c.*63A= XP_016879634.1:n.*63A=
XM_017024146.1:c.480-47A= XP_016879635.1:n.480-47A=
XM_024450563.1:c.*221A= XP_024306331.1:n.*221A=
NM_001080510.5:c.408-47A= MANE Select NP_001073979.3:n.408-47A=
NM_001206983.3:c.408-47A= NP_001193912.1:n.408-47A=
NM_001206984.3:c.408-47A= NP_001193913.1:n.408-47A=
NM_001206985.3:c.207-47A= NP_001193914.1:n.207-47A=
NM_001206986.3:c.207-47A= NP_001193915.1:n.207-47A=
NM_001206987.3:c.207-47A= NP_001193916.1:n.207-47A=
NM_001302703.2:c.408-47A= NP_001289632.1:n.408-47A=
NM_001302704.2:c.207-47A= NP_001289633.1:n.207-47A=
NM_001302705.2:c.396-47A= NP_001289634.1:n.396-47A=
NM_001378348.1:c.408-47A= NP_001365277.1:n.408-47A=
NM_001378349.1:c.408-47A= NP_001365278.1:n.408-47A=
NM_001378350.1:c.396-47A= NP_001365279.1:n.396-47A=
NM_001378351.1:c.396-47A= NP_001365280.1:n.396-47A=
NM_001378352.1:c.396-47A= NP_001365281.1:n.396-47A=
NM_001378353.1:c.396-47A= NP_001365282.1:n.396-47A=
NM_001378354.1:c.207-47A= NP_001365283.1:n.207-47A=