Canonical Allele Identifier: CA2324927595

Gene: CYP4F22

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540708C= , CM000681.2:g.15540708C=	GRCh38
NC_000019.9:g.15651519C= , CM000681.1:g.15651519C=	GRCh37
NC_000019.8:g.15512519C=	NCBI36
NG_007987.1:g.37184C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.930C= MANE Select	ENSP00000269703.1:p.Leu310=
ENST00000269703.7:c.930C=	ENSP00000269703.1:p.Leu310=
ENST00000601005.2:c.930C=	ENSP00000469866.1:p.Leu310=
NM_173483.3:c.930C=	NP_775754.2:p.Leu310=
XM_011527692.1:c.930C=	XP_011525994.1:p.Leu310=
XM_011527693.1:c.930C=	XP_011525995.1:p.Leu310=
XM_011527692.2:c.930C=	XP_011525994.1:p.Leu310=
XM_011527693.2:c.930C=	XP_011525995.1:p.Leu310=
NM_173483.4:c.930C= MANE Select	NP_775754.2:p.Leu310=