Canonical Allele Identifier: CA404567421

Gene: CYP4F11

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402119.9:c.1336G>C MANE Select	ENSP00000384588.2:p.Asp446His
ENST00000248041.12:c.1336G>C	ENSP00000248041.6:p.Asp446His
ENST00000326742.12:c.1271G>C	ENSP00000319859.7:p.Arg424Pro
ENST00000402119.8:c.1336G>C	ENSP00000384588.2:p.Asp446His
ENST00000591841.1:c.361G>C	ENSP00000476972.1:p.Asp121His
ENST00000620614.4:c.1271G>C	ENSP00000481243.1:p.Arg424Pro
NM_001128932.1:c.1336G>C	NP_001122404.1:p.Asp446His
NM_021187.3:c.1336G>C	NP_067010.3:p.Asp446His
XM_011528156.1:c.1282G>C	XP_011526458.1:p.Asp428His
NM_001128932.2:c.1336G>C	NP_001122404.1:p.Asp446His
NM_021187.4:c.1336G>C MANE Select	NP_067010.3:p.Asp446His