Canonical Allele Identifier: CA2325113659
Community Standard Title: NM_021187.4(CYP4F11):c.1336G= (p.Asp446=)
Gene: CYP4F11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15914366C= , CM000681.2:g.15914366C= GRCh38
NC_000019.9:g.16025176C= , CM000681.1:g.16025176C= GRCh37
NC_000019.8:g.15886176C= NCBI36
NG_008335.1:g.25501G=

Transcript Alleles

HGVS Amino-acid Change
NM_021187.4:c.1336G= MANE Select NP_067010.3:p.Asp446=
ENST00000402119.9:c.1336G= MANE Select ENSP00000384588.2:p.Asp446=
NM_001128932.1:c.1336G= NP_001122404.1:p.Asp446=
NM_001128932.2:c.1336G= NP_001122404.1:p.Asp446=
NM_021187.3:c.1336G= NP_067010.3:p.Asp446=
ENST00000248041.12:c.1336G= ENSP00000248041.6:p.Asp446=
ENST00000326742.12:c.1271G= ENSP00000319859.7:p.Arg424=
ENST00000402119.8:c.1336G= ENSP00000384588.2:p.Asp446=
ENST00000591841.1:c.361G= ENSP00000476972.1:p.Asp121=
ENST00000620614.4:c.1271G= ENSP00000481243.1:p.Arg424=
XM_011528156.1:c.1282G= XP_011526458.1:p.Asp428=