Canonical Allele Identifier: CA401188428

Gene: METTL23

Linked Data

• MyVariant Identifiers: chr17:g.74729471T>G (hg19) ; chr17:g.76733389T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76733389T>G , CM000679.2:g.76733389T>G	GRCh38
NC_000017.10:g.74729471T>G , CM000679.1:g.74729471T>G	GRCh37
NC_000017.9:g.72241066T>G	NCBI36
NG_032905.1:g.9023A>C , LRG_640:g.9023A>C
NG_041790.1:g.11560T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341249.11:c.407+12T>G MANE Select	ENSP00000341543.5:n.407+12T>G
ENST00000341249.10:c.407+12T>G	ENSP00000341543.5:n.407+12T>G
ENST00000586200.1:c.50+12T>G	ENSP00000465959.1:n.50+12T>G
ENST00000586738.5:c.411+8T>G	ENSP00000468386.1:n.411+8T>G
ENST00000586752.5:c.206+12T>G	ENSP00000466203.1:n.206+12T>G
ENST00000587459.1:c.238+174T>G	ENSP00000466829.1:n.238+174T>G
ENST00000588302.5:c.210+8T>G	ENSP00000468704.1:n.210+8T>G
ENST00000588563.5:c.407+12T>G	ENSP00000467503.1:n.407+12T>G
ENST00000588783.5:c.411+8T>G	ENSP00000466938.1:n.411+8T>G
ENST00000588822.1:c.206+12T>G	ENSP00000465430.1:n.206+12T>G
ENST00000589581.1:n.503+12T>G
ENST00000589977.5:c.419T>G	ENSP00000464965.1:p.Met140Arg
ENST00000590964.5:c.206+12T>G	ENSP00000465890.1:n.206+12T>G
ENST00000591571.5:c.218T>G	ENSP00000466614.1:p.Met73Arg
ENST00000592849.5:c.407+12T>G	ENSP00000467527.1:n.407+12T>G
ENST00000615984.4:c.407+12T>G	ENSP00000482599.1:n.407+12T>G
NM_001080510.4:c.407+12T>G	NP_001073979.3:n.407+12T>G
NM_001206983.2:c.407+12T>G	NP_001193912.1:n.407+12T>G
NM_001206984.2:c.407+12T>G	NP_001193913.1:n.407+12T>G
NM_001206985.2:c.206+12T>G	NP_001193914.1:n.206+12T>G
NM_001206986.2:c.206+12T>G	NP_001193915.1:n.206+12T>G
NM_001206987.2:c.206+12T>G	NP_001193916.1:n.206+12T>G
NM_001302703.1:c.407+12T>G	NP_001289632.1:n.407+12T>G
NM_001302704.1:c.206+12T>G	NP_001289633.1:n.206+12T>G
NM_001302705.1:c.395+12T>G	NP_001289634.1:n.395+12T>G
NR_038193.2:n.434+12T>G
XM_006721673.2:c.443+12T>G	XP_006721736.1:n.443+12T>G
XM_006721674.2:c.407+12T>G	XP_006721737.1:n.407+12T>G
XM_006721675.1:c.395+12T>G	XP_006721738.1:n.395+12T>G
XM_006721676.2:c.395+12T>G	XP_006721739.1:n.395+12T>G
XM_006721678.2:c.395+12T>G	XP_006721741.1:n.395+12T>G
XM_006721679.2:c.374+12T>G	XP_006721742.1:n.374+12T>G
XM_006721680.2:c.206+12T>G	XP_006721743.1:n.206+12T>G
XM_011524282.1:c.395+12T>G	XP_011522584.1:n.395+12T>G
XM_006721674.3:c.407+12T>G	XP_006721737.1:n.407+12T>G
XM_006721676.3:c.395+12T>G	XP_006721739.1:n.395+12T>G
XM_006721678.4:c.395+12T>G	XP_006721741.1:n.395+12T>G
XM_006721679.3:c.374+12T>G	XP_006721742.1:n.374+12T>G
XM_017024145.2:c.407T>G	XP_016879634.1:p.Met136Arg
XM_017024146.1:c.479+12T>G	XP_016879635.1:n.479+12T>G
XM_024450563.1:c.*136T>G	XP_024306331.1:n.*136T>G
NM_001080510.5:c.407+12T>G MANE Select	NP_001073979.3:n.407+12T>G
NM_001206983.3:c.407+12T>G	NP_001193912.1:n.407+12T>G
NM_001206984.3:c.407+12T>G	NP_001193913.1:n.407+12T>G
NM_001206985.3:c.206+12T>G	NP_001193914.1:n.206+12T>G
NM_001206986.3:c.206+12T>G	NP_001193915.1:n.206+12T>G
NM_001206987.3:c.206+12T>G	NP_001193916.1:n.206+12T>G
NM_001302703.2:c.407+12T>G	NP_001289632.1:n.407+12T>G
NM_001302704.2:c.206+12T>G	NP_001289633.1:n.206+12T>G
NM_001302705.2:c.395+12T>G	NP_001289634.1:n.395+12T>G
NM_001378348.1:c.407+12T>G	NP_001365277.1:n.407+12T>G
NM_001378349.1:c.407+12T>G	NP_001365278.1:n.407+12T>G
NM_001378350.1:c.395+12T>G	NP_001365279.1:n.395+12T>G
NM_001378351.1:c.395+12T>G	NP_001365280.1:n.395+12T>G
NM_001378352.1:c.395+12T>G	NP_001365281.1:n.395+12T>G
NM_001378353.1:c.395+12T>G	NP_001365282.1:n.395+12T>G
NM_001378354.1:c.206+12T>G	NP_001365283.1:n.206+12T>G