Canonical Allele Identifier: CA343176635

Gene: FMO3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171092659A>G , CM000663.2:g.171092659A>G	GRCh38
NC_000001.10:g.171061800A>G , CM000663.1:g.171061800A>G	GRCh37
NC_000001.9:g.169328424A>G	NCBI36
NG_012690.1:g.6783A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001002294.3:c.1A>G MANE Select	NP_001002294.1:p.Met1Val
ENST00000367755.9:c.1A>G MANE Select	ENSP00000356729.4:p.Met1Val
NM_001002294.2:c.1A>G	NP_001002294.1:p.Met1Val
NM_001319173.1:c.-187A>G	NP_001306102.1:n.-187A>G
NM_001319173.2:c.-187A>G	NP_001306102.1:n.-187A>G
NM_001319174.1:c.1A>G	NP_001306103.1:p.Met1Val
NM_001319174.2:c.1A>G	NP_001306103.1:p.Met1Val
NM_006894.5:c.1A>G	NP_008825.4:p.Met1Val
NM_006894.6:c.1A>G	NP_008825.4:p.Met1Val
ENST00000367755.8:c.1A>G	ENSP00000356729.4:p.Met1Val
ENST00000472784.5:c.1A>G	ENSP00000476963.1:p.Met1Val
ENST00000479749.1:c.1A>G	ENSP00000477451.1:p.Met1Val
ENST00000530212.5:n.88A>G
ENST00000534514.1:n.84A>G
XM_005245044.1:c.1A>G	XP_005245101.1:p.Met1Val
XM_011509345.1:c.-187A>G	XP_011507647.1:n.-187A>G
XM_011509345.3:c.-187A>G	XP_011507647.1:n.-187A>G
XM_011509346.1:c.-187A>G	XP_011507648.1:n.-187A>G