Canonical Allele Identifier: CA1140803244

Gene: FMO3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171107811C= , CM000663.2:g.171107811C=	GRCh38
NC_000001.10:g.171076952C= , CM000663.1:g.171076952C=	GRCh37
NC_000001.9:g.169343576C=	NCBI36
NG_012690.1:g.21935C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367755.9:c.458C= MANE Select	ENSP00000356729.4:p.Pro153=
ENST00000367755.8:c.458C=	ENSP00000356729.4:p.Pro153=
ENST00000479749.1:c.458C=	ENSP00000477451.1:p.Pro153=
NM_001002294.2:c.458C=	NP_001002294.1:p.Pro153=
NM_006894.5:c.458C=	NP_008825.4:p.Pro153=
XM_005245044.1:c.269C=	XP_005245101.1:p.Pro90=
XM_011509345.1:c.398C=	XP_011507647.1:p.Pro133=
XM_011509346.1:c.398C=	XP_011507648.1:p.Pro133=
NM_001319173.1:c.398C=	NP_001306102.1:p.Pro133=
NM_001319174.1:c.269C=	NP_001306103.1:p.Pro90=
XM_011509345.3:c.398C=	XP_011507647.1:p.Pro133=
XM_024454365.1:c.-90C=	XP_024310133.1:n.-90C=
NM_001002294.3:c.458C= MANE Select	NP_001002294.1:p.Pro153=
NM_001319173.2:c.398C=	NP_001306102.1:p.Pro133=
NM_001319174.2:c.269C=	NP_001306103.1:p.Pro90=
NM_006894.6:c.458C=	NP_008825.4:p.Pro153=