Canonical Allele Identifier: CA1140803241

Gene: FMO3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171103850G= , CM000663.2:g.171103850G=	GRCh38
NC_000001.10:g.171072991G= , CM000663.1:g.171072991G=	GRCh37
NC_000001.9:g.169339615G=	NCBI36
NG_012690.1:g.17974G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001002294.3:c.198G= MANE Select	NP_001002294.1:p.Met66=
ENST00000367755.9:c.198G= MANE Select	ENSP00000356729.4:p.Met66=
NM_001002294.2:c.198G=	NP_001002294.1:p.Met66=
NM_001319173.1:c.138G=	NP_001306102.1:p.Met46=
NM_001319173.2:c.138G=	NP_001306102.1:p.Met46=
NM_001319174.1:c.133-3825G=	NP_001306103.1:n.133-3825G=
NM_001319174.2:c.133-3825G=	NP_001306103.1:n.133-3825G=
NM_006894.5:c.198G=	NP_008825.4:p.Met66=
NM_006894.6:c.198G=	NP_008825.4:p.Met66=
ENST00000367755.8:c.198G=	ENSP00000356729.4:p.Met66=
ENST00000472784.5:c.*178G=	ENSP00000476963.1:n.*178G=
ENST00000478457.1:n.511G=
ENST00000479749.1:c.198G=	ENSP00000477451.1:p.Met66=
XM_005245044.1:c.133-3825G=	XP_005245101.1:n.133-3825G=
XM_011509345.1:c.138G=	XP_011507647.1:p.Met46=
XM_011509345.3:c.138G=	XP_011507647.1:p.Met46=
XM_011509346.1:c.138G=	XP_011507648.1:p.Met46=