Canonical Allele Identifier: CA2583119687
Gene: CYP4F3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15640940C>A , CM000681.2:g.15640940C>A GRCh38
NC_000019.9:g.15751750C>A , CM000681.1:g.15751750C>A GRCh37
NC_000019.8:g.15612750C>A NCBI36
NG_007964.1:g.5044C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221307.13:c.-7C>A MANE Select ENSP00000221307.6:n.-7C>A
ENST00000221307.12:c.-7C>A ENSP00000221307.6:n.-7C>A
ENST00000586182.6:c.-2+11C>A ENSP00000466395.1:n.-2+11C>A
ENST00000591058.5:c.-7C>A ENSP00000466988.1:n.-7C>A
ENST00000592279.6:n.44C>A
ENST00000620621.4:c.344-6112C>A ENSP00000478605.1:n.344-6112C>A
NM_000896.2:c.-7C>A NP_000887.2:n.-7C>A
NM_001199208.1:c.-7C>A NP_001186137.1:n.-7C>A
NM_001199209.1:c.-2+11C>A NP_001186138.1:n.-2+11C>A
NM_000896.3:c.-7C>A MANE Select NP_000887.2:n.-7C>A
NM_001199208.2:c.-7C>A NP_001186137.1:n.-7C>A
NM_001199209.2:c.-2+11C>A NP_001186138.1:n.-2+11C>A