Canonical Allele Identifier: CA2583147467

Gene: CYP4F2

Linked Data

• gnomAD v4: 19-15897335-A-AAC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897335_15897336insAC , CM000681.2:g.15897335_15897336insAC	GRCh38
NC_000019.9:g.16008145_16008146insAC , CM000681.1:g.16008145_16008146insAC	GRCh37
NC_000019.8:g.15869145_15869146insAC	NCBI36
NG_007971.2:g.5739_5740insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.198+78_198+79insGT MANE Select	ENSP00000221700.3:n.198+78_198+79insGT
ENST00000011989.11:c.198+78_198+79insGT	ENSP00000011989.8:n.198+78_198+79insGT
ENST00000221700.10:c.198+78_198+79insGT	ENSP00000221700.3:n.198+78_198+79insGT
ENST00000392846.7:n.49+690_49+691insGT
ENST00000586927.2:c.198+78_198+79insGT	ENSP00000465514.1:n.198+78_198+79insGT
ENST00000587671.2:c.198+78_198+79insGT	ENSP00000467443.2:n.198+78_198+79insGT
ENST00000608168.1:n.251+78_251+79insGT
NM_001082.4:c.198+78_198+79insGT	NP_001073.3:n.198+78_198+79insGT
NM_001082.5:c.198+78_198+79insGT MANE Select	NP_001073.3:n.198+78_198+79insGT