Canonical Allele Identifier: CA1139925021

Gene: FMO3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171107825G= , CM000663.2:g.171107825G=	GRCh38
NC_000001.10:g.171076966G= , CM000663.1:g.171076966G=	GRCh37
NC_000001.9:g.169343590G=	NCBI36
NG_012690.1:g.21949G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367755.9:c.472G= MANE Select	ENSP00000356729.4:p.Glu158=
ENST00000367755.8:c.472G=	ENSP00000356729.4:p.Glu158=
ENST00000479749.1:c.467+5G=	ENSP00000477451.1:n.467+5G=
NM_001002294.2:c.472G=	NP_001002294.1:p.Glu158=
NM_006894.5:c.472G=	NP_008825.4:p.Glu158=
XM_005245044.1:c.283G=	XP_005245101.1:p.Glu95=
XM_011509345.1:c.412G=	XP_011507647.1:p.Glu138=
XM_011509346.1:c.412G=	XP_011507648.1:p.Glu138=
NM_001319173.1:c.412G=	NP_001306102.1:p.Glu138=
NM_001319174.1:c.283G=	NP_001306103.1:p.Glu95=
XM_011509345.3:c.412G=	XP_011507647.1:p.Glu138=
XM_024454365.1:c.-76G=	XP_024310133.1:n.-76G=
NM_001002294.3:c.472G= MANE Select	NP_001002294.1:p.Glu158=
NM_001319173.2:c.412G=	NP_001306102.1:p.Glu138=
NM_001319174.2:c.283G=	NP_001306103.1:p.Glu95=
NM_006894.6:c.472G=	NP_008825.4:p.Glu158=