Canonical Allele Identifier: CA2583107944

Gene: CYP4F22

Linked Data

• gnomAD v4: 19-15540341-T-TTC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540345_15540346dup , CM000681.2:g.15540345_15540346dup	GRCh38
NC_000019.9:g.15651156_15651157dup , CM000681.1:g.15651156_15651157dup	GRCh37
NC_000019.8:g.15512156_15512157dup	NCBI36
NG_007987.1:g.36821_36822dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000269703.8:c.672-105_672-104dup MANE Select	ENSP00000269703.1:n.672-105_672-104dup
ENST00000269703.7:c.672-105_672-104dup	ENSP00000269703.1:n.672-105_672-104dup
ENST00000601005.2:c.672-105_672-104dup	ENSP00000469866.1:n.672-105_672-104dup
NM_173483.3:c.672-105_672-104dup	NP_775754.2:n.672-105_672-104dup
XM_011527692.1:c.672-105_672-104dup	XP_011525994.1:n.672-105_672-104dup
XM_011527693.1:c.672-105_672-104dup	XP_011525995.1:n.672-105_672-104dup
XM_011527692.2:c.672-105_672-104dup	XP_011525994.1:n.672-105_672-104dup
XM_011527693.2:c.672-105_672-104dup	XP_011525995.1:n.672-105_672-104dup
NM_173483.4:c.672-105_672-104dup MANE Select	NP_775754.2:n.672-105_672-104dup