Canonical Allele Identifier: CA1240622

Gene: FMO3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171110830G>A , CM000663.2:g.171110830G>A	GRCh38
NC_000001.10:g.171079971G>A , CM000663.1:g.171079971G>A	GRCh37
NC_000001.9:g.169346595G>A	NCBI36
NG_012690.1:g.24954G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001002294.3:c.660G>A MANE Select	NP_001002294.1:p.Val220=
ENST00000367755.9:c.660G>A MANE Select	ENSP00000356729.4:p.Val220=
NM_001002294.2:c.660G>A	NP_001002294.1:p.Val220=
NM_001319173.1:c.600G>A	NP_001306102.1:p.Val200=
NM_001319173.2:c.600G>A	NP_001306102.1:p.Val200=
NM_001319174.1:c.471G>A	NP_001306103.1:p.Val157=
NM_001319174.2:c.471G>A	NP_001306103.1:p.Val157=
NM_006894.5:c.660G>A	NP_008825.4:p.Val220=
NM_006894.6:c.660G>A	NP_008825.4:p.Val220=
ENST00000367755.8:c.660G>A	ENSP00000356729.4:p.Val220=
ENST00000479749.1:c.606G>A	ENSP00000477451.1:p.Val202=
XM_005245044.1:c.471G>A	XP_005245101.1:p.Val157=
XM_011509345.1:c.600G>A	XP_011507647.1:p.Val200=
XM_011509345.3:c.600G>A	XP_011507647.1:p.Val200=
XM_011509346.1:c.600G>A	XP_011507648.1:p.Val200=
XM_024454365.1:c.80+2609G>A	XP_024310133.1:n.80+2609G>A