Canonical Allele Identifier: CA1240579

Gene: FMO3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171108179G>C , CM000663.2:g.171108179G>C	GRCh38
NC_000001.10:g.171077320G>C , CM000663.1:g.171077320G>C	GRCh37
NC_000001.9:g.169343944G>C	NCBI36
NG_012690.1:g.22303G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001002294.3:c.585G>C MANE Select	NP_001002294.1:p.Ser195=
ENST00000367755.9:c.585G>C MANE Select	ENSP00000356729.4:p.Ser195=
NM_001002294.2:c.585G>C	NP_001002294.1:p.Ser195=
NM_001319173.1:c.525G>C	NP_001306102.1:p.Ser175=
NM_001319173.2:c.525G>C	NP_001306102.1:p.Ser175=
NM_001319174.1:c.396G>C	NP_001306103.1:p.Ser132=
NM_001319174.2:c.396G>C	NP_001306103.1:p.Ser132=
NM_006894.5:c.585G>C	NP_008825.4:p.Ser195=
NM_006894.6:c.585G>C	NP_008825.4:p.Ser195=
ENST00000367755.8:c.585G>C	ENSP00000356729.4:p.Ser195=
ENST00000479749.1:c.531G>C	ENSP00000477451.1:p.Ser177=
XM_005245044.1:c.396G>C	XP_005245101.1:p.Ser132=
XM_011509345.1:c.525G>C	XP_011507647.1:p.Ser175=
XM_011509345.3:c.525G>C	XP_011507647.1:p.Ser175=
XM_011509346.1:c.525G>C	XP_011507648.1:p.Ser175=
XM_024454365.1:c.38G>C	XP_024310133.1:p.Arg13Pro