Canonical Allele Identifier: CA891080842

Gene: FMO2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171209124_171209125dup , CM000663.2:g.171209124_171209125dup	GRCh38
NC_000001.10:g.171178263_171178264dup , CM000663.1:g.171178263_171178264dup	GRCh37
NC_000001.9:g.169444887_169444888dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209929.10:c.1587_1588dup MANE Select	ENSP00000209929.8:p.Cys530PhefsTer24
ENST00000209929.9:c.1587_1588dup	ENSP00000209929.8:p.Cys530PhefsTer24
ENST00000488431.1:n.579_580dup
ENST00000529935.5:c.1372_1373dup	ENSP00000487002.1:n.1372_1373dup
NM_001301347.1:c.927_928dup	NP_001288276.1:p.Cys310PhefsTer24
NM_001460.4:c.1587_1588dup	NP_001451.2:p.Cys530PhefsTer24
XR_426768.2:n.1704_1705dup
XR_921761.1:n.1704_1705dup
XR_922278.1:n.507+38461_507+38462dup
NM_001365900.1:c.1392_1393dup	NP_001352829.1:p.Cys465PhefsTer24
NR_158622.1:n.1607_1608dup
XR_001737072.2:n.1654_1655dup
XR_001738291.2:n.1306+38461_1306+38462dup
XR_921761.3:n.1654_1655dup
XR_922278.3:n.1306+38461_1306+38462dup
NM_001460.5:c.1587_1588dup MANE Select	NP_001451.2:p.Cys530PhefsTer24
NR_160266.1:n.1515_1516dup
NM_001301347.2:c.927_928dup	NP_001288276.1:p.Cys310PhefsTer24