Canonical Allele Identifier: CA2001561485

Gene: NNMT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.114298316A= , CM000673.2:g.114298316A=	GRCh38
NC_000011.9:g.114169038A= , CM000673.1:g.114169038A=	GRCh37
NC_000011.8:g.113674248A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713573.1:c.362+158A=	ENSP00000518865.1:n.362+158A=
ENST00000299964.4:c.362+158A= MANE Select	ENSP00000299964.3:n.362+158A=
ENST00000299964.3:c.362+158A=	ENSP00000299964.3:n.362+158A=
ENST00000535401.5:c.362+158A=	ENSP00000441434.1:n.362+158A=
ENST00000541090.1:n.188-13729A=
ENST00000541754.1:n.244+158A=
ENST00000542647.5:n.40+181A=
ENST00000545255.1:n.44+122A=
ENST00000546313.1:n.654A=
NM_006169.2:c.362+158A=	NP_006160.1:n.362+158A=
NM_001372045.1:c.362+158A=	NP_001358974.1:n.362+158A=
NM_001372046.1:c.362+158A=	NP_001358975.1:n.362+158A=
NM_001372047.1:c.362+158A=	NP_001358976.1:n.362+158A=
NM_006169.3:c.362+158A= MANE Select	NP_006160.1:n.362+158A=
NR_164073.1:n.581+158A=