Canonical Allele Identifier: CA343185298

Gene: FMO3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171108216G>C , CM000663.2:g.171108216G>C	GRCh38
NC_000001.10:g.171077357G>C , CM000663.1:g.171077357G>C	GRCh37
NC_000001.9:g.169343981G>C	NCBI36
NG_012690.1:g.22340G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001002294.3:c.622G>C MANE Select	NP_001002294.1:p.Glu208Gln
ENST00000367755.9:c.622G>C MANE Select	ENSP00000356729.4:p.Glu208Gln
NM_001002294.2:c.622G>C	NP_001002294.1:p.Glu208Gln
NM_001319173.1:c.562G>C	NP_001306102.1:p.Glu188Gln
NM_001319173.2:c.562G>C	NP_001306102.1:p.Glu188Gln
NM_001319174.1:c.433G>C	NP_001306103.1:p.Glu145Gln
NM_001319174.2:c.433G>C	NP_001306103.1:p.Glu145Gln
NM_006894.5:c.622G>C	NP_008825.4:p.Glu208Gln
NM_006894.6:c.622G>C	NP_008825.4:p.Glu208Gln
ENST00000367755.8:c.622G>C	ENSP00000356729.4:p.Glu208Gln
ENST00000479749.1:c.568G>C	ENSP00000477451.1:p.Glu190Gln
XM_005245044.1:c.433G>C	XP_005245101.1:p.Glu145Gln
XM_011509345.1:c.562G>C	XP_011507647.1:p.Glu188Gln
XM_011509345.3:c.562G>C	XP_011507647.1:p.Glu188Gln
XM_011509346.1:c.562G>C	XP_011507648.1:p.Glu188Gln
XM_024454365.1:c.75G>C	XP_024310133.1:p.Gln25His