Canonical Allele Identifier: CA1240851
Community Standard Title: NM_001002294.3(FMO3):c.1499G>A (p.Arg500Gln)
Gene: FMO3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171117342G>A , CM000663.2:g.171117342G>A GRCh38
NC_000001.10:g.171086482G>A , CM000663.1:g.171086482G>A GRCh37
NC_000001.9:g.169353106G>A NCBI36
NG_012690.1:g.31465G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001002294.3:c.1499G>A MANE Select NP_001002294.1:p.Arg500Gln
ENST00000367755.9:c.1499G>A MANE Select ENSP00000356729.4:p.Arg500Gln
NM_001002294.2:c.1499G>A NP_001002294.1:p.Arg500Gln
NM_001319173.1:c.1439G>A NP_001306102.1:p.Arg480Gln
NM_001319173.2:c.1439G>A NP_001306102.1:p.Arg480Gln
NM_001319174.1:c.1310G>A NP_001306103.1:p.Arg437Gln
NM_001319174.2:c.1310G>A NP_001306103.1:p.Arg437Gln
NM_006894.5:c.1499G>A NP_008825.4:p.Arg500Gln
NM_006894.6:c.1499G>A NP_008825.4:p.Arg500Gln
ENST00000367755.8:c.1499G>A ENSP00000356729.4:p.Arg500Gln
XM_005245044.1:c.1310G>A XP_005245101.1:p.Arg437Gln
XM_011509345.1:c.1439G>A XP_011507647.1:p.Arg480Gln
XM_011509345.3:c.1439G>A XP_011507647.1:p.Arg480Gln
XM_011509346.1:c.1439G>A XP_011507648.1:p.Arg480Gln
XM_024454365.1:c.752G>A XP_024310133.1:p.Arg251Gln