Canonical Allele Identifier: CA343188033

Gene: FMO3

Linked Data

• COSMIC: COSM3774420
• MyVariant Identifiers: chr1:g.171083401T>C (hg19) ; chr1:g.171114261T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171114261T>C , CM000663.2:g.171114261T>C	GRCh38
NC_000001.10:g.171083401T>C , CM000663.1:g.171083401T>C	GRCh37
NC_000001.9:g.169350025T>C	NCBI36
NG_012690.1:g.28384T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367755.9:c.1082T>C MANE Select	ENSP00000356729.4:p.Leu361Pro
ENST00000367755.8:c.1082T>C	ENSP00000356729.4:p.Leu361Pro
NM_001002294.2:c.1082T>C	NP_001002294.1:p.Leu361Pro
NM_006894.5:c.1082T>C	NP_008825.4:p.Leu361Pro
XM_005245044.1:c.893T>C	XP_005245101.1:p.Leu298Pro
XM_011509345.1:c.1022T>C	XP_011507647.1:p.Leu341Pro
XM_011509346.1:c.1022T>C	XP_011507648.1:p.Leu341Pro
NM_001319173.1:c.1022T>C	NP_001306102.1:p.Leu341Pro
NM_001319174.1:c.893T>C	NP_001306103.1:p.Leu298Pro
XM_011509345.3:c.1022T>C	XP_011507647.1:p.Leu341Pro
XM_024454365.1:c.335T>C	XP_024310133.1:p.Leu112Pro
NM_001002294.3:c.1082T>C MANE Select	NP_001002294.1:p.Leu361Pro
NM_001319173.2:c.1022T>C	NP_001306102.1:p.Leu341Pro
NM_001319174.2:c.893T>C	NP_001306103.1:p.Leu298Pro
NM_006894.6:c.1082T>C	NP_008825.4:p.Leu361Pro