Canonical Allele Identifier: CA343186581

Gene: FMO3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171110948A>G , CM000663.2:g.171110948A>G	GRCh38
NC_000001.10:g.171080089A>G , CM000663.1:g.171080089A>G	GRCh37
NC_000001.9:g.169346713A>G	NCBI36
NG_012690.1:g.25072A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001002294.3:c.778A>G MANE Select	NP_001002294.1:p.Met260Val
ENST00000367755.9:c.778A>G MANE Select	ENSP00000356729.4:p.Met260Val
NM_001002294.2:c.778A>G	NP_001002294.1:p.Met260Val
NM_001319173.1:c.718A>G	NP_001306102.1:p.Met240Val
NM_001319173.2:c.718A>G	NP_001306102.1:p.Met240Val
NM_001319174.1:c.589A>G	NP_001306103.1:p.Met197Val
NM_001319174.2:c.589A>G	NP_001306103.1:p.Met197Val
NM_006894.5:c.778A>G	NP_008825.4:p.Met260Val
NM_006894.6:c.778A>G	NP_008825.4:p.Met260Val
ENST00000367755.8:c.778A>G	ENSP00000356729.4:p.Met260Val
XM_005245044.1:c.589A>G	XP_005245101.1:p.Met197Val
XM_011509345.1:c.718A>G	XP_011507647.1:p.Met240Val
XM_011509345.3:c.718A>G	XP_011507647.1:p.Met240Val
XM_011509346.1:c.718A>G	XP_011507648.1:p.Met240Val
XM_024454365.1:c.80+2727A>G	XP_024310133.1:n.80+2727A>G