Canonical Allele Identifier: CA1140803249

Gene: FMO3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171114339G= , CM000663.2:g.171114339G=	GRCh38
NC_000001.10:g.171083479G= , CM000663.1:g.171083479G=	GRCh37
NC_000001.9:g.169350103G=	NCBI36
NG_012690.1:g.28462G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367755.9:c.1160G= MANE Select	ENSP00000356729.4:p.Arg387=
ENST00000367755.8:c.1160G=	ENSP00000356729.4:p.Arg387=
NM_001002294.2:c.1160G=	NP_001002294.1:p.Arg387=
NM_006894.5:c.1160G=	NP_008825.4:p.Arg387=
XM_005245044.1:c.971G=	XP_005245101.1:p.Arg324=
XM_011509345.1:c.1100G=	XP_011507647.1:p.Arg367=
XM_011509346.1:c.1100G=	XP_011507648.1:p.Arg367=
NM_001319173.1:c.1100G=	NP_001306102.1:p.Arg367=
NM_001319174.1:c.971G=	NP_001306103.1:p.Arg324=
XM_011509345.3:c.1100G=	XP_011507647.1:p.Arg367=
XM_024454365.1:c.413G=	XP_024310133.1:p.Arg138=
NM_001002294.3:c.1160G= MANE Select	NP_001002294.1:p.Arg387=
NM_001319173.2:c.1100G=	NP_001306102.1:p.Arg367=
NM_001319174.2:c.971G=	NP_001306103.1:p.Arg324=
NM_006894.6:c.1160G=	NP_008825.4:p.Arg387=