Canonical Allele Identifier: CA1140803239

Gene: FMO3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171103806G= , CM000663.2:g.171103806G=	GRCh38
NC_000001.10:g.171072947G= , CM000663.1:g.171072947G=	GRCh37
NC_000001.9:g.169339571G=	NCBI36
NG_012690.1:g.17930G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367755.9:c.154G= MANE Select	ENSP00000356729.4:p.Ala52=
ENST00000367755.8:c.154G=	ENSP00000356729.4:p.Ala52=
ENST00000472784.5:c.*134G=	ENSP00000476963.1:n.*134G=
ENST00000478457.1:n.467G=
ENST00000479749.1:c.154G=	ENSP00000477451.1:p.Ala52=
NM_001002294.2:c.154G=	NP_001002294.1:p.Ala52=
NM_006894.5:c.154G=	NP_008825.4:p.Ala52=
XM_005245044.1:c.133-3869G=	XP_005245101.1:n.133-3869G=
XM_011509345.1:c.94G=	XP_011507647.1:p.Ala32=
XM_011509346.1:c.94G=	XP_011507648.1:p.Ala32=
NM_001319173.1:c.94G=	NP_001306102.1:p.Ala32=
NM_001319174.1:c.133-3869G=	NP_001306103.1:n.133-3869G=
XM_011509345.3:c.94G=	XP_011507647.1:p.Ala32=
NM_001002294.3:c.154G= MANE Select	NP_001002294.1:p.Ala52=
NM_001319173.2:c.94G=	NP_001306102.1:p.Ala32=
NM_001319174.2:c.133-3869G=	NP_001306103.1:n.133-3869G=
NM_006894.6:c.154G=	NP_008825.4:p.Ala52=