Canonical Allele Identifier: CA2324977518

Gene: CYP4F3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15641027T= , CM000681.2:g.15641027T=	GRCh38
NC_000019.9:g.15751837T= , CM000681.1:g.15751837T=	GRCh37
NC_000019.8:g.15612837T=	NCBI36
NG_007964.1:g.5131T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221307.13:c.-2+82T= MANE Select	ENSP00000221307.6:n.-2+82T=
ENST00000221307.12:c.-2+82T=	ENSP00000221307.6:n.-2+82T=
ENST00000586182.6:c.-2+98T=	ENSP00000466395.1:n.-2+98T=
ENST00000591058.5:c.-2+82T=	ENSP00000466988.1:n.-2+82T=
ENST00000592279.6:n.49+82T=
ENST00000620621.4:c.344-6025T=	ENSP00000478605.1:n.344-6025T=
NM_000896.2:c.-2+82T=	NP_000887.2:n.-2+82T=
NM_001199208.1:c.-2+82T=	NP_001186137.1:n.-2+82T=
NM_001199209.1:c.-2+98T=	NP_001186138.1:n.-2+98T=
NM_000896.3:c.-2+82T= MANE Select	NP_000887.2:n.-2+82T=
NM_001199208.2:c.-2+82T=	NP_001186137.1:n.-2+82T=
NM_001199209.2:c.-2+98T=	NP_001186138.1:n.-2+98T=