Canonical Allele Identifier: CA2324977562
Gene: CYP4F3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15641126A= , CM000681.2:g.15641126A= GRCh38
NC_000019.9:g.15751936A= , CM000681.1:g.15751936A= GRCh37
NC_000019.8:g.15612936A= NCBI36
NG_007964.1:g.5230A=

Transcript Alleles

HGVS Amino-acid change
ENST00000221307.13:c.-2+181A= MANE Select ENSP00000221307.6:n.-2+181A=
ENST00000221307.12:c.-2+181A= ENSP00000221307.6:n.-2+181A=
ENST00000586182.6:c.-2+197A= ENSP00000466395.1:n.-2+197A=
ENST00000591058.5:c.-2+181A= ENSP00000466988.1:n.-2+181A=
ENST00000592279.6:n.49+181A=
ENST00000620621.4:c.344-5926A= ENSP00000478605.1:n.344-5926A=
NM_000896.2:c.-2+181A= NP_000887.2:n.-2+181A=
NM_001199208.1:c.-2+181A= NP_001186137.1:n.-2+181A=
NM_001199209.1:c.-2+197A= NP_001186138.1:n.-2+197A=
NM_000896.3:c.-2+181A= MANE Select NP_000887.2:n.-2+181A=
NM_001199208.2:c.-2+181A= NP_001186137.1:n.-2+181A=
NM_001199209.2:c.-2+197A= NP_001186138.1:n.-2+197A=