Canonical Allele Identifier: CA2583147582

Gene: CYP4F2

Linked Data

• gnomAD v4: 19-15897670-C-CCT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15897672_15897673dup , CM000681.2:g.15897672_15897673dup	GRCh38
NC_000019.9:g.16008482_16008483dup , CM000681.1:g.16008482_16008483dup	GRCh37
NC_000019.8:g.15869482_15869483dup	NCBI36
NG_007971.2:g.5403_5404dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221700.11:c.-1-60_-1-59dup MANE Select	ENSP00000221700.3:n.-1-60_-1-59dup
ENST00000011989.11:c.-1-60_-1-59dup	ENSP00000011989.8:n.-1-60_-1-59dup
ENST00000221700.10:c.-1-60_-1-59dup	ENSP00000221700.3:n.-1-60_-1-59dup
ENST00000392846.7:n.49+354_49+355dup
ENST00000586927.2:c.-61_-60dup	ENSP00000465514.1:n.-61_-60dup
ENST00000587671.2:c.-1-60_-1-59dup	ENSP00000467443.2:n.-1-60_-1-59dup
ENST00000608168.1:n.53-60_53-59dup
NM_001082.4:c.-1-60_-1-59dup	NP_001073.3:n.-1-60_-1-59dup
NM_001082.5:c.-1-60_-1-59dup MANE Select	NP_001073.3:n.-1-60_-1-59dup