Canonical Allele Identifier: CA2324927928

Gene: CYP4F22

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540729_15540775delinsCCCCCTGGAATTGCTGGCCTCCCGAGGGCTGGCCTCCCGAGGAATTG , CM000681.2:g.15540729_15540775delinsCCCCCTGGAATTGCTGGCCTCCCGAGGGCTGGCCTCCCGAGGAATTG	GRCh38
NC_000019.9:g.15651540_15651586delinsCCCCCTGGAATTGCTGGCCTCCCGAGGGCTGGCCTCCCGAGGAATTG , CM000681.1:g.15651540_15651586delinsCCCCCTGGAATTGCTGGCCTCCCGAGGGCTGGCCTCCCGAGGAATTG	GRCh37
NC_000019.8:g.15512540_15512586delinsCCCCCTGGAATTGCTGGCCTCCCGAGGGCTGGCCTCCCGAGGAATTG	NCBI36
NG_007987.1:g.37205_37251delinsCCCCCTGGAATTGCTGGCCTCCCGAGGGCTGGCCTCCCGAGGAATTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+12_939+58delinsCCCCCTGGAATTGCTGGCCTCCCGAGGGCTGGCCTCCCGAGGAATTG MANE Select	ENSP00000269703.1:n.939+12_939+58delinsCCCCCTGGAATTGCTGGCCTCC...
ENST00000269703.7:c.939+12_939+58delinsCCCCCTGGAATTGCTGGCCTCCCGAGGGCTGGCCTCCCGAGGAATTG	ENSP00000269703.1:n.939+12_939+58delinsCCCCCTGGAATTGCTGGCCTCC...
ENST00000601005.2:c.939+12_939+58delinsCCCCCTGGAATTGCTGGCCTCCCGAGGGCTGGCCTCCCGAGGAATTG	ENSP00000469866.1:n.939+12_939+58delinsCCCCCTGGAATTGCTGGCCTCC...
NM_173483.3:c.939+12_939+58delinsCCCCCTGGAATTGCTGGCCTCCCGAGGGCTGGCCTCCCGAGGAATTG	NP_775754.2:n.939+12_939+58delinsCCCCCTGGAATTGCTGGCCTCCCGAGGG...
XM_011527692.1:c.939+12_939+58delinsCCCCCTGGAATTGCTGGCCTCCCGAGGGCTGGCCTCCCGAGGAATTG	XP_011525994.1:n.939+12_939+58delinsCCCCCTGGAATTGCTGGCCTCCCGA...
XM_011527693.1:c.939+12_939+58delinsCCCCCTGGAATTGCTGGCCTCCCGAGGGCTGGCCTCCCGAGGAATTG	XP_011525995.1:n.939+12_939+58delinsCCCCCTGGAATTGCTGGCCTCCCGA...
XM_011527692.2:c.939+12_939+58delinsCCCCCTGGAATTGCTGGCCTCCCGAGGGCTGGCCTCCCGAGGAATTG	XP_011525994.1:n.939+12_939+58delinsCCCCCTGGAATTGCTGGCCTCCCGA...
XM_011527693.2:c.939+12_939+58delinsCCCCCTGGAATTGCTGGCCTCCCGAGGGCTGGCCTCCCGAGGAATTG	XP_011525995.1:n.939+12_939+58delinsCCCCCTGGAATTGCTGGCCTCCCGA...
NM_173483.4:c.939+12_939+58delinsCCCCCTGGAATTGCTGGCCTCCCGAGGGCTGGCCTCCCGAGGAATTG MANE Select	NP_775754.2:n.939+12_939+58delinsCCCCCTGGAATTGCTGGCCTCCCGAGGG...