Canonical Allele Identifier: CA2324984232

Gene: CYP4F3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15652911G= , CM000681.2:g.15652911G=	GRCh38
NC_000019.9:g.15763721G= , CM000681.1:g.15763721G=	GRCh37
NC_000019.8:g.15624721G=	NCBI36
NG_007964.1:g.17015G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000896.3:c.1074G= MANE Select	NP_000887.2:p.Val358=
ENST00000221307.13:c.1074G= MANE Select	ENSP00000221307.6:p.Val358=
NM_000896.2:c.1074G=	NP_000887.2:p.Val358=
NM_001199208.1:c.1074G=	NP_001186137.1:p.Val358=
NM_001199208.2:c.1074G=	NP_001186137.1:p.Val358=
NM_001199209.1:c.1074G=	NP_001186138.1:p.Val358=
NM_001199209.2:c.1074G=	NP_001186138.1:p.Val358=
NM_001369696.1:c.1074G=	NP_001356625.1:p.Val358=
ENST00000221307.12:c.1074G=	ENSP00000221307.6:p.Val358=
ENST00000585846.1:c.1074G=	ENSP00000468105.1:p.Val358=
ENST00000586182.6:c.1074G=	ENSP00000466395.1:p.Val358=
ENST00000591058.5:c.1074G=	ENSP00000466988.1:p.Val358=
ENST00000592279.6:n.1215G=
ENST00000592424.1:c.467G=	ENSP00000476546.1:n.467G=
ENST00000620621.4:c.1074G=	ENSP00000478605.1:p.Val358=
XM_005259911.3:c.627G=	XP_005259968.1:p.Val209=
XM_005259911.5:c.627G=	XP_005259968.1:p.Val209=
XM_011528014.1:c.627G=	XP_011526316.1:p.Val209=
XM_011528014.3:c.627G=	XP_011526316.1:p.Val209=
XM_017026815.1:c.1074G=	XP_016882304.1:p.Val358=