Canonical Allele Identifier: CA2324927471
Gene: CYP4F22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540637C= , CM000681.2:g.15540637C= GRCh38
NC_000019.9:g.15651448C= , CM000681.1:g.15651448C= GRCh37
NC_000019.8:g.15512448C= NCBI36
NG_007987.1:g.37113C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.859C= MANE Select ENSP00000269703.1:p.Arg287=
ENST00000269703.7:c.859C= ENSP00000269703.1:p.Arg287=
ENST00000601005.2:c.859C= ENSP00000469866.1:p.Arg287=
NM_173483.3:c.859C= NP_775754.2:p.Arg287=
XM_011527692.1:c.859C= XP_011525994.1:p.Arg287=
XM_011527693.1:c.859C= XP_011525995.1:p.Arg287=
XM_011527692.2:c.859C= XP_011525994.1:p.Arg287=
XM_011527693.2:c.859C= XP_011525995.1:p.Arg287=
NM_173483.4:c.859C= MANE Select NP_775754.2:p.Arg287=