Canonical Allele Identifier: CA1139925025

Gene: FMO3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171114102A= , CM000663.2:g.171114102A=	GRCh38
NC_000001.10:g.171083242A= , CM000663.1:g.171083242A=	GRCh37
NC_000001.9:g.169349866A=	NCBI36
NG_012690.1:g.28225A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367755.9:c.923A= MANE Select	ENSP00000356729.4:p.Glu308=
ENST00000367755.8:c.923A=	ENSP00000356729.4:p.Glu308=
NM_001002294.2:c.923A=	NP_001002294.1:p.Glu308=
NM_006894.5:c.923A=	NP_008825.4:p.Glu308=
XM_005245044.1:c.734A=	XP_005245101.1:p.Glu245=
XM_011509345.1:c.863A=	XP_011507647.1:p.Glu288=
XM_011509346.1:c.863A=	XP_011507648.1:p.Glu288=
NM_001319173.1:c.863A=	NP_001306102.1:p.Glu288=
NM_001319174.1:c.734A=	NP_001306103.1:p.Glu245=
XM_011509345.3:c.863A=	XP_011507647.1:p.Glu288=
XM_024454365.1:c.176A=	XP_024310133.1:p.Glu59=
NM_001002294.3:c.923A= MANE Select	NP_001002294.1:p.Glu308=
NM_001319173.2:c.863A=	NP_001306102.1:p.Glu288=
NM_001319174.2:c.734A=	NP_001306103.1:p.Glu245=
NM_006894.6:c.923A=	NP_008825.4:p.Glu308=