Canonical Allele Identifier: CA2583145447
Gene: CYP4F2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15879450del , CM000681.2:g.15879450del GRCh38
NC_000019.9:g.15990260del , CM000681.1:g.15990260del GRCh37
NC_000019.8:g.15851260del NCBI36
NG_007971.2:g.23627del

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.1315-20del MANE Select ENSP00000221700.3:n.1315-20del
ENST00000011989.11:c.1315-20del ENSP00000011989.8:n.1315-20del
ENST00000221700.10:c.1315-20del ENSP00000221700.3:n.1315-20del
ENST00000392846.7:n.1258-20del
ENST00000589654.2:c.103-20del
NM_001082.4:c.1315-20del NP_001073.3:n.1315-20del
NM_001082.5:c.1315-20del MANE Select NP_001073.3:n.1315-20del