Canonical Allele Identifier: CA1240861

Gene: FMO3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171117373C>T , CM000663.2:g.171117373C>T	GRCh38
NC_000001.10:g.171086513C>T , CM000663.1:g.171086513C>T	GRCh37
NC_000001.9:g.169353137C>T	NCBI36
NG_012690.1:g.31496C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001002294.3:c.1530C>T MANE Select	NP_001002294.1:p.Phe510=
ENST00000367755.9:c.1530C>T MANE Select	ENSP00000356729.4:p.Phe510=
NM_001002294.2:c.1530C>T	NP_001002294.1:p.Phe510=
NM_001319173.1:c.1470C>T	NP_001306102.1:p.Phe490=
NM_001319173.2:c.1470C>T	NP_001306102.1:p.Phe490=
NM_001319174.1:c.1341C>T	NP_001306103.1:p.Phe447=
NM_001319174.2:c.1341C>T	NP_001306103.1:p.Phe447=
NM_006894.5:c.1530C>T	NP_008825.4:p.Phe510=
NM_006894.6:c.1530C>T	NP_008825.4:p.Phe510=
ENST00000367755.8:c.1530C>T	ENSP00000356729.4:p.Phe510=
XM_005245044.1:c.1341C>T	XP_005245101.1:p.Phe447=
XM_011509345.1:c.1470C>T	XP_011507647.1:p.Phe490=
XM_011509345.3:c.1470C>T	XP_011507647.1:p.Phe490=
XM_011509346.1:c.1470C>T	XP_011507648.1:p.Phe490=
XM_024454365.1:c.783C>T	XP_024310133.1:p.Phe261=