Canonical Allele Identifier: CA2324927428

Gene: CYP4F22

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540621_15540624delinsACGG , CM000681.2:g.15540621_15540624delinsACGG	GRCh38
NC_000019.9:g.15651432_15651435delinsACGG , CM000681.1:g.15651432_15651435delinsACGG	GRCh37
NC_000019.8:g.15512432_15512435delinsACGG	NCBI36
NG_007987.1:g.37097_37100delinsACGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.843_846delinsACGG MANE Select	ENSP00000269703.1:p.Glu281=
ENST00000269703.7:c.843_846delinsACGG	ENSP00000269703.1:p.Glu281=
ENST00000601005.2:c.843_846delinsACGG	ENSP00000469866.1:p.Glu281=
NM_173483.3:c.843_846delinsACGG	NP_775754.2:p.Glu281=
XM_011527692.1:c.843_846delinsACGG	XP_011525994.1:p.Glu281=
XM_011527693.1:c.843_846delinsACGG	XP_011525995.1:p.Glu281=
XM_011527692.2:c.843_846delinsACGG	XP_011525994.1:p.Glu281=
XM_011527693.2:c.843_846delinsACGG	XP_011525995.1:p.Glu281=
NM_173483.4:c.843_846delinsACGG MANE Select	NP_775754.2:p.Glu281=