Canonical Allele Identifier: CA2324977471
Gene: CYP4F3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15640923G= , CM000681.2:g.15640923G= GRCh38
NC_000019.9:g.15751733G= , CM000681.1:g.15751733G= GRCh37
NC_000019.8:g.15612733G= NCBI36
NG_007964.1:g.5027G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221307.13:c.-24G= MANE Select ENSP00000221307.6:n.-24G=
ENST00000221307.12:c.-24G= ENSP00000221307.6:n.-24G=
ENST00000586182.6:c.-8G= ENSP00000466395.1:n.-8G=
ENST00000591058.5:c.-24G= ENSP00000466988.1:n.-24G=
ENST00000592279.6:n.27G=
ENST00000620621.4:c.344-6129G= ENSP00000478605.1:n.344-6129G=
NM_000896.2:c.-24G= NP_000887.2:n.-24G=
NM_001199208.1:c.-24G= NP_001186137.1:n.-24G=
NM_001199209.1:c.-8G= NP_001186138.1:n.-8G=
NM_000896.3:c.-24G= MANE Select NP_000887.2:n.-24G=
NM_001199208.2:c.-24G= NP_001186137.1:n.-24G=
NM_001199209.2:c.-8G= NP_001186138.1:n.-8G=