Canonical Allele Identifier: CA343180055

Gene: FMO3

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171103834A>C , CM000663.2:g.171103834A>C	GRCh38
NC_000001.10:g.171072975A>C , CM000663.1:g.171072975A>C	GRCh37
NC_000001.9:g.169339599A>C	NCBI36
NG_012690.1:g.17958A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367755.9:c.182A>C MANE Select	ENSP00000356729.4:p.Asn61Thr
ENST00000367755.8:c.182A>C	ENSP00000356729.4:p.Asn61Thr
ENST00000472784.5:c.*162A>C	ENSP00000476963.1:n.*162A>C
ENST00000478457.1:n.495A>C
ENST00000479749.1:c.182A>C	ENSP00000477451.1:p.Asn61Thr
NM_001002294.2:c.182A>C	NP_001002294.1:p.Asn61Thr
NM_006894.5:c.182A>C	NP_008825.4:p.Asn61Thr
XM_005245044.1:c.133-3841A>C	XP_005245101.1:n.133-3841A>C
XM_011509345.1:c.122A>C	XP_011507647.1:p.Asn41Thr
XM_011509346.1:c.122A>C	XP_011507648.1:p.Asn41Thr
NM_001319173.1:c.122A>C	NP_001306102.1:p.Asn41Thr
NM_001319174.1:c.133-3841A>C	NP_001306103.1:n.133-3841A>C
XM_011509345.3:c.122A>C	XP_011507647.1:p.Asn41Thr
NM_001002294.3:c.182A>C MANE Select	NP_001002294.1:p.Asn61Thr
NM_001319173.2:c.122A>C	NP_001306102.1:p.Asn41Thr
NM_001319174.2:c.133-3841A>C	NP_001306103.1:n.133-3841A>C
NM_006894.6:c.182A>C	NP_008825.4:p.Asn61Thr