Canonical Allele Identifier: CA32506461

Gene: FMO3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171117100G>A , CM000663.2:g.171117100G>A	GRCh38
NC_000001.10:g.171086240G>A , CM000663.1:g.171086240G>A	GRCh37
NC_000001.9:g.169352864G>A	NCBI36
NG_012690.1:g.31223G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001002294.3:c.1257G>A MANE Select	NP_001002294.1:p.Trp419Ter
ENST00000367755.9:c.1257G>A MANE Select	ENSP00000356729.4:p.Trp419Ter
NM_001002294.2:c.1257G>A	NP_001002294.1:p.Trp419Ter
NM_001319173.1:c.1197G>A	NP_001306102.1:p.Trp399Ter
NM_001319173.2:c.1197G>A	NP_001306102.1:p.Trp399Ter
NM_001319174.1:c.1068G>A	NP_001306103.1:p.Trp356Ter
NM_001319174.2:c.1068G>A	NP_001306103.1:p.Trp356Ter
NM_006894.5:c.1257G>A	NP_008825.4:p.Trp419Ter
NM_006894.6:c.1257G>A	NP_008825.4:p.Trp419Ter
ENST00000367755.8:c.1257G>A	ENSP00000356729.4:p.Trp419Ter
XM_005245044.1:c.1068G>A	XP_005245101.1:p.Trp356Ter
XM_011509345.1:c.1197G>A	XP_011507647.1:p.Trp399Ter
XM_011509345.3:c.1197G>A	XP_011507647.1:p.Trp399Ter
XM_011509346.1:c.1197G>A	XP_011507648.1:p.Trp399Ter
XM_024454365.1:c.510G>A	XP_024310133.1:p.Trp170Ter