Canonical Allele Identifier: CA1240477

Gene: FMO3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171103803A>G , CM000663.2:g.171103803A>G	GRCh38
NC_000001.10:g.171072944A>G , CM000663.1:g.171072944A>G	GRCh37
NC_000001.9:g.169339568A>G	NCBI36
NG_012690.1:g.17927A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001002294.3:c.151A>G MANE Select	NP_001002294.1:p.Arg51Gly
ENST00000367755.9:c.151A>G MANE Select	ENSP00000356729.4:p.Arg51Gly
NM_001002294.2:c.151A>G	NP_001002294.1:p.Arg51Gly
NM_001319173.1:c.91A>G	NP_001306102.1:p.Arg31Gly
NM_001319173.2:c.91A>G	NP_001306102.1:p.Arg31Gly
NM_001319174.1:c.133-3872A>G	NP_001306103.1:n.133-3872A>G
NM_001319174.2:c.133-3872A>G	NP_001306103.1:n.133-3872A>G
NM_006894.5:c.151A>G	NP_008825.4:p.Arg51Gly
NM_006894.6:c.151A>G	NP_008825.4:p.Arg51Gly
ENST00000367755.8:c.151A>G	ENSP00000356729.4:p.Arg51Gly
ENST00000472784.5:c.*131A>G	ENSP00000476963.1:n.*131A>G
ENST00000478457.1:n.464A>G
ENST00000479749.1:c.151A>G	ENSP00000477451.1:p.Arg51Gly
XM_005245044.1:c.133-3872A>G	XP_005245101.1:n.133-3872A>G
XM_011509345.1:c.91A>G	XP_011507647.1:p.Arg31Gly
XM_011509345.3:c.91A>G	XP_011507647.1:p.Arg31Gly
XM_011509346.1:c.91A>G	XP_011507648.1:p.Arg31Gly