Canonical Allele Identifier: CA1240502

Gene: FMO3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171103974G>T , CM000663.2:g.171103974G>T	GRCh38
NC_000001.10:g.171073115G>T , CM000663.1:g.171073115G>T	GRCh37
NC_000001.9:g.169339739G>T	NCBI36
NG_012690.1:g.18098G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001002294.3:c.321+1G>T MANE Select	NP_001002294.1:n.321+1G>T
ENST00000367755.9:c.321+1G>T MANE Select	ENSP00000356729.4:n.321+1G>T
NM_001002294.2:c.321+1G>T	NP_001002294.1:n.321+1G>T
NM_001319173.1:c.261+1G>T	NP_001306102.1:n.261+1G>T
NM_001319173.2:c.261+1G>T	NP_001306102.1:n.261+1G>T
NM_001319174.1:c.133-3701G>T	NP_001306103.1:n.133-3701G>T
NM_001319174.2:c.133-3701G>T	NP_001306103.1:n.133-3701G>T
NM_006894.5:c.321+1G>T	NP_008825.4:n.321+1G>T
NM_006894.6:c.321+1G>T	NP_008825.4:n.321+1G>T
ENST00000367755.8:c.321+1G>T	ENSP00000356729.4:n.321+1G>T
ENST00000472784.5:c.*301+1G>T	ENSP00000476963.1:n.*301+1G>T
ENST00000478457.1:n.634+1G>T
ENST00000479749.1:c.321+1G>T	ENSP00000477451.1:n.321+1G>T
XM_005245044.1:c.133-3701G>T	XP_005245101.1:n.133-3701G>T
XM_011509345.1:c.261+1G>T	XP_011507647.1:n.261+1G>T
XM_011509345.3:c.261+1G>T	XP_011507647.1:n.261+1G>T
XM_011509346.1:c.261+1G>T	XP_011507648.1:n.261+1G>T