Canonical Allele Identifier: CA1140803238

Gene: FMO3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171092752G= , CM000663.2:g.171092752G=	GRCh38
NC_000001.10:g.171061893G= , CM000663.1:g.171061893G=	GRCh37
NC_000001.9:g.169328517G=	NCBI36
NG_012690.1:g.6876G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367755.9:c.94G= MANE Select	ENSP00000356729.4:p.Glu32=
ENST00000367755.8:c.94G=	ENSP00000356729.4:p.Glu32=
ENST00000472784.5:c.94G=	ENSP00000476963.1:p.Glu32=
ENST00000479749.1:c.94G=	ENSP00000477451.1:p.Glu32=
ENST00000530212.5:n.181G=
ENST00000534514.1:n.177G=
NM_001002294.2:c.94G=	NP_001002294.1:p.Glu32=
NM_006894.5:c.94G=	NP_008825.4:p.Glu32=
XM_005245044.1:c.94G=	XP_005245101.1:p.Glu32=
XM_011509345.1:c.-94G=	XP_011507647.1:n.-94G=
XM_011509346.1:c.-94G=	XP_011507648.1:n.-94G=
NM_001319173.1:c.-94G=	NP_001306102.1:n.-94G=
NM_001319174.1:c.94G=	NP_001306103.1:p.Glu32=
XM_011509345.3:c.-94G=	XP_011507647.1:n.-94G=
NM_001002294.3:c.94G= MANE Select	NP_001002294.1:p.Glu32=
NM_001319173.2:c.-94G=	NP_001306102.1:n.-94G=
NM_001319174.2:c.94G=	NP_001306103.1:p.Glu32=
NM_006894.6:c.94G=	NP_008825.4:p.Glu32=