Canonical Allele Identifier: CA2325105613

Gene: CYP4F2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897586A= , CM000681.2:g.15897586A=	GRCh38
NC_000019.9:g.16008396A= , CM000681.1:g.16008396A=	GRCh37
NC_000019.8:g.15869396A=	NCBI36
NG_007971.2:g.5489T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.26T= MANE Select	ENSP00000221700.3:p.Leu9=
ENST00000011989.11:c.26T=	ENSP00000011989.8:p.Leu9=
ENST00000221700.10:c.26T=	ENSP00000221700.3:p.Leu9=
ENST00000392846.7:n.49+440T=
ENST00000586927.2:c.26T=	ENSP00000465514.1:p.Leu9=
ENST00000587671.2:c.26T=	ENSP00000467443.2:p.Leu9=
ENST00000608168.1:n.79T=
NM_001082.4:c.26T=	NP_001073.3:p.Leu9=
NM_001082.5:c.26T= MANE Select	NP_001073.3:p.Leu9=