Canonical Allele Identifier: CA1240586

Gene: FMO3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171108207C>T , CM000663.2:g.171108207C>T	GRCh38
NC_000001.10:g.171077348C>T , CM000663.1:g.171077348C>T	GRCh37
NC_000001.9:g.169343972C>T	NCBI36
NG_012690.1:g.22331C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001002294.3:c.613C>T MANE Select	NP_001002294.1:p.Arg205Cys
ENST00000367755.9:c.613C>T MANE Select	ENSP00000356729.4:p.Arg205Cys
NM_001002294.2:c.613C>T	NP_001002294.1:p.Arg205Cys
NM_001319173.1:c.553C>T	NP_001306102.1:p.Arg185Cys
NM_001319173.2:c.553C>T	NP_001306102.1:p.Arg185Cys
NM_001319174.1:c.424C>T	NP_001306103.1:p.Arg142Cys
NM_001319174.2:c.424C>T	NP_001306103.1:p.Arg142Cys
NM_006894.5:c.613C>T	NP_008825.4:p.Arg205Cys
NM_006894.6:c.613C>T	NP_008825.4:p.Arg205Cys
ENST00000367755.8:c.613C>T	ENSP00000356729.4:p.Arg205Cys
ENST00000479749.1:c.559C>T	ENSP00000477451.1:p.Arg187Cys
XM_005245044.1:c.424C>T	XP_005245101.1:p.Arg142Cys
XM_011509345.1:c.553C>T	XP_011507647.1:p.Arg185Cys
XM_011509345.3:c.553C>T	XP_011507647.1:p.Arg185Cys
XM_011509346.1:c.553C>T	XP_011507648.1:p.Arg185Cys
XM_024454365.1:c.66C>T	XP_024310133.1:p.Ala22=