Canonical Allele Identifier: CA1240494

Gene: FMO3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171103897T>C , CM000663.2:g.171103897T>C	GRCh38
NC_000001.10:g.171073038T>C , CM000663.1:g.171073038T>C	GRCh37
NC_000001.9:g.169339662T>C	NCBI36
NG_012690.1:g.18021T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001002294.3:c.245T>C MANE Select	NP_001002294.1:p.Met82Thr
ENST00000367755.9:c.245T>C MANE Select	ENSP00000356729.4:p.Met82Thr
NM_001002294.2:c.245T>C	NP_001002294.1:p.Met82Thr
NM_001319173.1:c.185T>C	NP_001306102.1:p.Met62Thr
NM_001319173.2:c.185T>C	NP_001306102.1:p.Met62Thr
NM_001319174.1:c.133-3778T>C	NP_001306103.1:n.133-3778T>C
NM_001319174.2:c.133-3778T>C	NP_001306103.1:n.133-3778T>C
NM_006894.5:c.245T>C	NP_008825.4:p.Met82Thr
NM_006894.6:c.245T>C	NP_008825.4:p.Met82Thr
ENST00000367755.8:c.245T>C	ENSP00000356729.4:p.Met82Thr
ENST00000472784.5:c.*225T>C	ENSP00000476963.1:n.*225T>C
ENST00000478457.1:n.558T>C
ENST00000479749.1:c.245T>C	ENSP00000477451.1:p.Met82Thr
XM_005245044.1:c.133-3778T>C	XP_005245101.1:n.133-3778T>C
XM_011509345.1:c.185T>C	XP_011507647.1:p.Met62Thr
XM_011509345.3:c.185T>C	XP_011507647.1:p.Met62Thr
XM_011509346.1:c.185T>C	XP_011507648.1:p.Met62Thr