Canonical Allele Identifier: CA343185311

Gene: FMO3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171108219C>T , CM000663.2:g.171108219C>T	GRCh38
NC_000001.10:g.171077360C>T , CM000663.1:g.171077360C>T	GRCh37
NC_000001.9:g.169343984C>T	NCBI36
NG_012690.1:g.22343C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001002294.3:c.625C>T MANE Select	NP_001002294.1:p.Gln209Ter
ENST00000367755.9:c.625C>T MANE Select	ENSP00000356729.4:p.Gln209Ter
NM_001002294.2:c.625C>T	NP_001002294.1:p.Gln209Ter
NM_001319173.1:c.565C>T	NP_001306102.1:p.Gln189Ter
NM_001319173.2:c.565C>T	NP_001306102.1:p.Gln189Ter
NM_001319174.1:c.436C>T	NP_001306103.1:p.Gln146Ter
NM_001319174.2:c.436C>T	NP_001306103.1:p.Gln146Ter
NM_006894.5:c.625C>T	NP_008825.4:p.Gln209Ter
NM_006894.6:c.625C>T	NP_008825.4:p.Gln209Ter
ENST00000367755.8:c.625C>T	ENSP00000356729.4:p.Gln209Ter
ENST00000479749.1:c.571C>T	ENSP00000477451.1:p.Gln191Ter
XM_005245044.1:c.436C>T	XP_005245101.1:p.Gln146Ter
XM_011509345.1:c.565C>T	XP_011507647.1:p.Gln189Ter
XM_011509345.3:c.565C>T	XP_011507647.1:p.Gln189Ter
XM_011509346.1:c.565C>T	XP_011507648.1:p.Gln189Ter
XM_024454365.1:c.78C>T	XP_024310133.1:p.Asn26=