Canonical Allele Identifier: CA2324927486

Gene: CYP4F22

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540645G= , CM000681.2:g.15540645G=	GRCh38
NC_000019.9:g.15651456G= , CM000681.1:g.15651456G=	GRCh37
NC_000019.8:g.15512456G=	NCBI36
NG_007987.1:g.37121G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.867G= MANE Select	ENSP00000269703.1:p.Gln289=
ENST00000269703.7:c.867G=	ENSP00000269703.1:p.Gln289=
ENST00000601005.2:c.867G=	ENSP00000469866.1:p.Gln289=
NM_173483.3:c.867G=	NP_775754.2:p.Gln289=
XM_011527692.1:c.867G=	XP_011525994.1:p.Gln289=
XM_011527693.1:c.867G=	XP_011525995.1:p.Gln289=
XM_011527692.2:c.867G=	XP_011525994.1:p.Gln289=
XM_011527693.2:c.867G=	XP_011525995.1:p.Gln289=
NM_173483.4:c.867G= MANE Select	NP_775754.2:p.Gln289=