Canonical Allele Identifier: CA1240616

Gene: FMO3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171110797G>A , CM000663.2:g.171110797G>A	GRCh38
NC_000001.10:g.171079938G>A , CM000663.1:g.171079938G>A	GRCh37
NC_000001.9:g.169346562G>A	NCBI36
NG_012690.1:g.24921G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001002294.3:c.628-1G>A MANE Select	NP_001002294.1:n.628-1G>A
ENST00000367755.9:c.628-1G>A MANE Select	ENSP00000356729.4:n.628-1G>A
NM_001002294.2:c.628-1G>A	NP_001002294.1:n.628-1G>A
NM_001319173.1:c.568-1G>A	NP_001306102.1:n.568-1G>A
NM_001319173.2:c.568-1G>A	NP_001306102.1:n.568-1G>A
NM_001319174.1:c.439-1G>A	NP_001306103.1:n.439-1G>A
NM_001319174.2:c.439-1G>A	NP_001306103.1:n.439-1G>A
NM_006894.5:c.628-1G>A	NP_008825.4:n.628-1G>A
NM_006894.6:c.628-1G>A	NP_008825.4:n.628-1G>A
ENST00000367755.8:c.628-1G>A	ENSP00000356729.4:n.628-1G>A
ENST00000479749.1:c.574-1G>A	ENSP00000477451.1:n.574-1G>A
XM_005245044.1:c.439-1G>A	XP_005245101.1:n.439-1G>A
XM_011509345.1:c.568-1G>A	XP_011507647.1:n.568-1G>A
XM_011509345.3:c.568-1G>A	XP_011507647.1:n.568-1G>A
XM_011509346.1:c.568-1G>A	XP_011507648.1:n.568-1G>A
XM_024454365.1:c.80+2576G>A	XP_024310133.1:n.80+2576G>A