Canonical Allele Identifier: CA343180001

Gene: FMO3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171103822C>G , CM000663.2:g.171103822C>G	GRCh38
NC_000001.10:g.171072963C>G , CM000663.1:g.171072963C>G	GRCh37
NC_000001.9:g.169339587C>G	NCBI36
NG_012690.1:g.17946C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001002294.3:c.170C>G MANE Select	NP_001002294.1:p.Ser57Ter
ENST00000367755.9:c.170C>G MANE Select	ENSP00000356729.4:p.Ser57Ter
NM_001002294.2:c.170C>G	NP_001002294.1:p.Ser57Ter
NM_001319173.1:c.110C>G	NP_001306102.1:p.Ser37Ter
NM_001319173.2:c.110C>G	NP_001306102.1:p.Ser37Ter
NM_001319174.1:c.133-3853C>G	NP_001306103.1:n.133-3853C>G
NM_001319174.2:c.133-3853C>G	NP_001306103.1:n.133-3853C>G
NM_006894.5:c.170C>G	NP_008825.4:p.Ser57Ter
NM_006894.6:c.170C>G	NP_008825.4:p.Ser57Ter
ENST00000367755.8:c.170C>G	ENSP00000356729.4:p.Ser57Ter
ENST00000472784.5:c.*150C>G	ENSP00000476963.1:n.*150C>G
ENST00000478457.1:n.483C>G
ENST00000479749.1:c.170C>G	ENSP00000477451.1:p.Ser57Ter
XM_005245044.1:c.133-3853C>G	XP_005245101.1:n.133-3853C>G
XM_011509345.1:c.110C>G	XP_011507647.1:p.Ser37Ter
XM_011509345.3:c.110C>G	XP_011507647.1:p.Ser37Ter
XM_011509346.1:c.110C>G	XP_011507648.1:p.Ser37Ter