Canonical Allele Identifier: CA2325105614
Gene: CYP4F2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897587G= , CM000681.2:g.15897587G= GRCh38
NC_000019.9:g.16008397G= , CM000681.1:g.16008397G= GRCh37
NC_000019.8:g.15869397G= NCBI36
NG_007971.2:g.5488C=

Transcript Alleles

HGVS Amino-acid change
ENST00000221700.11:c.25C= MANE Select ENSP00000221700.3:p.Leu9=
ENST00000011989.11:c.25C= ENSP00000011989.8:p.Leu9=
ENST00000221700.10:c.25C= ENSP00000221700.3:p.Leu9=
ENST00000392846.7:n.49+439C=
ENST00000586927.2:c.25C= ENSP00000465514.1:p.Leu9=
ENST00000587671.2:c.25C= ENSP00000467443.2:p.Leu9=
ENST00000608168.1:n.78C=
NM_001082.4:c.25C= NP_001073.3:p.Leu9=
NM_001082.5:c.25C= MANE Select NP_001073.3:p.Leu9=