Canonical Allele Identifier: CA2583147418
Gene: CYP4F2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15897326del , CM000681.2:g.15897326del GRCh38
NC_000019.9:g.16008136del , CM000681.1:g.16008136del GRCh37
NC_000019.8:g.15869136del NCBI36
NG_007971.2:g.5751del

Transcript Alleles

HGVS Amino-acid Change
ENST00000221700.11:c.198+90del MANE Select ENSP00000221700.3:n.198+90del
ENST00000011989.11:c.198+90del ENSP00000011989.8:n.198+90del
ENST00000221700.10:c.198+90del ENSP00000221700.3:n.198+90del
ENST00000392846.7:n.49+702del
ENST00000586927.2:c.198+90del ENSP00000465514.1:n.198+90del
ENST00000587671.2:c.198+90del ENSP00000467443.2:n.198+90del
ENST00000608168.1:n.251+90del
NM_001082.4:c.198+90del NP_001073.3:n.198+90del
NM_001082.5:c.198+90del MANE Select NP_001073.3:n.198+90del