Canonical Allele Identifier: CA2325105532

Gene: CYP4F2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897433A= , CM000681.2:g.15897433A=	GRCh38
NC_000019.9:g.16008243A= , CM000681.1:g.16008243A=	GRCh37
NC_000019.8:g.15869243A=	NCBI36
NG_007971.2:g.5642T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.179T= MANE Select	ENSP00000221700.3:p.Phe60=
ENST00000011989.11:c.179T=	ENSP00000011989.8:p.Phe60=
ENST00000221700.10:c.179T=	ENSP00000221700.3:p.Phe60=
ENST00000392846.7:n.49+593T=
ENST00000586927.2:c.179T=	ENSP00000465514.1:p.Phe60=
ENST00000587671.2:c.179T=	ENSP00000467443.2:p.Phe60=
ENST00000608168.1:n.232T=
NM_001082.4:c.179T=	NP_001073.3:p.Phe60=
NM_001082.5:c.179T= MANE Select	NP_001073.3:p.Phe60=