Canonical Allele Identifier: CA2813739250

Gene: CYP4F22

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540649dup , CM000681.2:g.15540649dup	GRCh38
NC_000019.9:g.15651460dup , CM000681.1:g.15651460dup	GRCh37
NC_000019.8:g.15512460dup	NCBI36
NG_007987.1:g.37125dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.871dup MANE Select	ENSP00000269703.1:p.Ala291GlyfsTer6
ENST00000269703.7:c.871dup	ENSP00000269703.1:p.Ala291GlyfsTer6
ENST00000601005.2:c.871dup	ENSP00000469866.1:p.Ala291GlyfsTer6
NM_173483.3:c.871dup	NP_775754.2:p.Ala291GlyfsTer6
XM_011527692.1:c.871dup	XP_011525994.1:p.Ala291GlyfsTer6
XM_011527693.1:c.871dup	XP_011525995.1:p.Ala291GlyfsTer6
XM_011527692.2:c.871dup	XP_011525994.1:p.Ala291GlyfsTer6
XM_011527693.2:c.871dup	XP_011525995.1:p.Ala291GlyfsTer6
NM_173483.4:c.871dup MANE Select	NP_775754.2:p.Ala291GlyfsTer6