Canonical Allele Identifier: CA502068995

Gene: METTL23

Linked Data

• MyVariant Identifiers: chr17:g.74729376T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76733294T>C , CM000679.2:g.76733294T>C	GRCh38
NC_000017.10:g.74729376T>C , CM000679.1:g.74729376T>C	GRCh37
NC_000017.9:g.72240971T>C	NCBI36
NG_032905.1:g.9118A>G , LRG_640:g.9118A>G
NG_041790.1:g.11465T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341249.11:c.324T>C MANE Select	ENSP00000341543.5:p.Asp108=
ENST00000341249.10:c.324T>C	ENSP00000341543.5:p.Asp108=
ENST00000586200.1:c.-34T>C	ENSP00000465959.1:n.-34T>C
ENST00000586738.5:c.324T>C	ENSP00000468386.1:p.Asp108=
ENST00000586752.5:c.123T>C	ENSP00000466203.1:p.Asp41=
ENST00000587459.1:c.238+79T>C	ENSP00000466829.1:n.238+79T>C
ENST00000588302.5:c.123T>C	ENSP00000468704.1:p.Asp41=
ENST00000588563.5:c.324T>C	ENSP00000467503.1:p.Asp108=
ENST00000588783.5:c.324T>C	ENSP00000466938.1:p.Asp108=
ENST00000588822.1:c.123T>C	ENSP00000465430.1:p.Asp41=
ENST00000588964.1:c.123T>C	ENSP00000467101.1:p.Asp41=
ENST00000589581.1:n.420T>C
ENST00000589977.5:c.324T>C	ENSP00000464965.1:p.Asp108=
ENST00000590964.5:c.123T>C	ENSP00000465890.1:p.Asp41=
ENST00000591571.5:c.123T>C	ENSP00000466614.1:p.Asp41=
ENST00000592849.5:c.324T>C	ENSP00000467527.1:p.Asp108=
ENST00000615984.4:c.324T>C	ENSP00000482599.1:p.Asp108=
NM_001080510.4:c.324T>C	NP_001073979.3:p.Asp108=
NM_001206983.2:c.324T>C	NP_001193912.1:p.Asp108=
NM_001206984.2:c.324T>C	NP_001193913.1:p.Asp108=
NM_001206985.2:c.123T>C	NP_001193914.1:p.Asp41=
NM_001206986.2:c.123T>C	NP_001193915.1:p.Asp41=
NM_001206987.2:c.123T>C	NP_001193916.1:p.Asp41=
NM_001302703.1:c.324T>C	NP_001289632.1:p.Asp108=
NM_001302704.1:c.123T>C	NP_001289633.1:p.Asp41=
NM_001302705.1:c.312T>C	NP_001289634.1:p.Asp104=
NR_038193.2:n.351T>C
XM_006721673.2:c.360T>C	XP_006721736.1:p.Asp120=
XM_006721674.2:c.324T>C	XP_006721737.1:p.Asp108=
XM_006721675.1:c.312T>C	XP_006721738.1:p.Asp104=
XM_006721676.2:c.312T>C	XP_006721739.1:p.Asp104=
XM_006721678.2:c.312T>C	XP_006721741.1:p.Asp104=
XM_006721679.2:c.291T>C	XP_006721742.1:p.Asp97=
XM_006721680.2:c.123T>C	XP_006721743.1:p.Asp41=
XM_011524282.1:c.312T>C	XP_011522584.1:p.Asp104=
XM_006721674.3:c.324T>C	XP_006721737.1:p.Asp108=
XM_006721676.3:c.312T>C	XP_006721739.1:p.Asp104=
XM_006721678.4:c.312T>C	XP_006721741.1:p.Asp104=
XM_006721679.3:c.291T>C	XP_006721742.1:p.Asp97=
XM_017024145.2:c.312T>C	XP_016879634.1:p.Asp104=
XM_017024146.1:c.396T>C	XP_016879635.1:p.Asp132=
XM_024450563.1:c.*41T>C	XP_024306331.1:n.*41T>C
NM_001080510.5:c.324T>C MANE Select	NP_001073979.3:p.Asp108=
NM_001206983.3:c.324T>C	NP_001193912.1:p.Asp108=
NM_001206984.3:c.324T>C	NP_001193913.1:p.Asp108=
NM_001206985.3:c.123T>C	NP_001193914.1:p.Asp41=
NM_001206986.3:c.123T>C	NP_001193915.1:p.Asp41=
NM_001206987.3:c.123T>C	NP_001193916.1:p.Asp41=
NM_001302703.2:c.324T>C	NP_001289632.1:p.Asp108=
NM_001302704.2:c.123T>C	NP_001289633.1:p.Asp41=
NM_001302705.2:c.312T>C	NP_001289634.1:p.Asp104=
NM_001378348.1:c.324T>C	NP_001365277.1:p.Asp108=
NM_001378349.1:c.324T>C	NP_001365278.1:p.Asp108=
NM_001378350.1:c.312T>C	NP_001365279.1:p.Asp104=
NM_001378351.1:c.312T>C	NP_001365280.1:p.Asp104=
NM_001378352.1:c.312T>C	NP_001365281.1:p.Asp104=
NM_001378353.1:c.312T>C	NP_001365282.1:p.Asp104=
NM_001378354.1:c.123T>C	NP_001365283.1:p.Asp41=