Canonical Allele Identifier: CA2325101832

Gene: CYP4F2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15889455A= , CM000681.2:g.15889455A=	GRCh38
NC_000019.9:g.16000265A= , CM000681.1:g.16000265A=	GRCh37
NC_000019.8:g.15861265A=	NCBI36
NG_007971.2:g.13620T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.886T= MANE Select	ENSP00000221700.3:p.Leu296=
ENST00000011989.11:c.886T=	ENSP00000011989.8:p.Leu296=
ENST00000221700.10:c.886T=	ENSP00000221700.3:p.Leu296=
ENST00000392846.7:n.829T=
ENST00000587671.2:c.*471T=	ENSP00000467443.2:n.*471T=
NM_001082.4:c.886T=	NP_001073.3:p.Leu296=
NM_001082.5:c.886T= MANE Select	NP_001073.3:p.Leu296=