Canonical Allele Identifier: CA2324927461

Gene: CYP4F22

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540633_15540634delinsAC , CM000681.2:g.15540633_15540634delinsAC	GRCh38
NC_000019.9:g.15651444_15651445delinsAC , CM000681.1:g.15651444_15651445delinsAC	GRCh37
NC_000019.8:g.15512444_15512445delinsAC	NCBI36
NG_007987.1:g.37109_37110delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.855_856delinsAC MANE Select	ENSP00000269703.1:p.Ala285=
ENST00000269703.7:c.855_856delinsAC	ENSP00000269703.1:p.Ala285=
ENST00000601005.2:c.855_856delinsAC	ENSP00000469866.1:p.Ala285=
NM_173483.3:c.855_856delinsAC	NP_775754.2:p.Ala285=
XM_011527692.1:c.855_856delinsAC	XP_011525994.1:p.Ala285=
XM_011527693.1:c.855_856delinsAC	XP_011525995.1:p.Ala285=
XM_011527692.2:c.855_856delinsAC	XP_011525994.1:p.Ala285=
XM_011527693.2:c.855_856delinsAC	XP_011525995.1:p.Ala285=
NM_173483.4:c.855_856delinsAC MANE Select	NP_775754.2:p.Ala285=