Canonical Allele Identifier: CA1240816

Gene: FMO3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171117165T>C , CM000663.2:g.171117165T>C	GRCh38
NC_000001.10:g.171086305T>C , CM000663.1:g.171086305T>C	GRCh37
NC_000001.9:g.169352929T>C	NCBI36
NG_012690.1:g.31288T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001002294.3:c.1322T>C MANE Select	NP_001002294.1:p.Ile441Thr
ENST00000367755.9:c.1322T>C MANE Select	ENSP00000356729.4:p.Ile441Thr
NM_001002294.2:c.1322T>C	NP_001002294.1:p.Ile441Thr
NM_001319173.1:c.1262T>C	NP_001306102.1:p.Ile421Thr
NM_001319173.2:c.1262T>C	NP_001306102.1:p.Ile421Thr
NM_001319174.1:c.1133T>C	NP_001306103.1:p.Ile378Thr
NM_001319174.2:c.1133T>C	NP_001306103.1:p.Ile378Thr
NM_006894.5:c.1322T>C	NP_008825.4:p.Ile441Thr
NM_006894.6:c.1322T>C	NP_008825.4:p.Ile441Thr
ENST00000367755.8:c.1322T>C	ENSP00000356729.4:p.Ile441Thr
XM_005245044.1:c.1133T>C	XP_005245101.1:p.Ile378Thr
XM_011509345.1:c.1262T>C	XP_011507647.1:p.Ile421Thr
XM_011509345.3:c.1262T>C	XP_011507647.1:p.Ile421Thr
XM_011509346.1:c.1262T>C	XP_011507648.1:p.Ile421Thr
XM_024454365.1:c.575T>C	XP_024310133.1:p.Ile192Thr