Canonical Allele Identifier: CA10608769

Gene: FMO3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171090963G>A , CM000663.2:g.171090963G>A	GRCh38
NC_000001.10:g.171060104G>A , CM000663.1:g.171060104G>A	GRCh37
NC_000001.9:g.169326728G>A	NCBI36
NG_012690.1:g.5087G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001002294.3:c.-25G>A MANE Select	NP_001002294.1:n.-25G>A
ENST00000367755.9:c.-25G>A MANE Select	ENSP00000356729.4:n.-25G>A
NM_001002294.2:c.-25G>A	NP_001002294.1:n.-25G>A
NM_001319173.1:c.-195G>A	NP_001306102.1:n.-195G>A
NM_001319173.2:c.-195G>A	NP_001306102.1:n.-195G>A
NM_001319174.1:c.-25G>A	NP_001306103.1:n.-25G>A
NM_001319174.2:c.-25G>A	NP_001306103.1:n.-25G>A
NM_006894.5:c.-8G>A	NP_008825.4:n.-8G>A
NM_006894.6:c.-8G>A	NP_008825.4:n.-8G>A
ENST00000367755.8:c.-25G>A	ENSP00000356729.4:n.-25G>A
ENST00000472784.5:c.-25G>A	ENSP00000476963.1:n.-25G>A
ENST00000479749.1:c.-25G>A	ENSP00000477451.1:n.-25G>A
ENST00000530212.5:n.63G>A
ENST00000534514.1:n.59G>A
XM_005245044.1:c.-25G>A	XP_005245101.1:n.-25G>A
XM_011509345.1:c.-212G>A	XP_011507647.1:n.-212G>A
XM_011509345.3:c.-212G>A	XP_011507647.1:n.-212G>A
XM_011509346.1:c.-195G>A	XP_011507648.1:n.-195G>A