Canonical Allele Identifier: CA404572660
Gene: CYP4F2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879389C>T , CM000681.2:g.15879389C>T GRCh38
NC_000019.9:g.15990199C>T , CM000681.1:g.15990199C>T GRCh37
NC_000019.8:g.15851199C>T NCBI36
NG_007971.2:g.23686G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.1354G>A MANE Select ENSP00000221700.3:p.Glu452Lys
ENST00000011989.11:c.1354G>A ENSP00000011989.8:p.Glu452Lys
ENST00000221700.10:c.1354G>A ENSP00000221700.3:p.Glu452Lys
ENST00000392846.7:n.1297G>A
ENST00000589654.2:c.142G>A
NM_001082.4:c.1354G>A NP_001073.3:p.Glu452Lys
NM_001082.5:c.1354G>A MANE Select NP_001073.3:p.Glu452Lys