Canonical Allele Identifier: CA2324977455

Gene: CYP4F3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15640905G= , CM000681.2:g.15640905G=	GRCh38
NC_000019.9:g.15751715G= , CM000681.1:g.15751715G=	GRCh37
NC_000019.8:g.15612715G=	NCBI36
NG_007964.1:g.5009G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221307.13:c.-42G= MANE Select	ENSP00000221307.6:n.-42G=
ENST00000221307.12:c.-42G=	ENSP00000221307.6:n.-42G=
ENST00000586182.6:c.-26G=	ENSP00000466395.1:n.-26G=
ENST00000591058.5:c.-42G=	ENSP00000466988.1:n.-42G=
ENST00000592279.6:n.9G=
ENST00000620621.4:c.344-6147G=	ENSP00000478605.1:n.344-6147G=
NM_000896.2:c.-42G=	NP_000887.2:n.-42G=
NM_001199208.1:c.-42G=	NP_001186137.1:n.-42G=
NM_001199209.1:c.-26G=	NP_001186138.1:n.-26G=
NM_000896.3:c.-42G= MANE Select	NP_000887.2:n.-42G=
NM_001199208.2:c.-42G=	NP_001186137.1:n.-42G=
NM_001199209.2:c.-26G=	NP_001186138.1:n.-26G=