Canonical Allele Identifier: CA2090489265
Gene: PHF11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.49528579C= , CM000675.2:g.49528579C= GRCh38
NC_000013.10:g.50102715C= , CM000675.1:g.50102715C= GRCh37
NC_000013.9:g.49000716C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000378319.8:c.910C= MANE Select ENSP00000367570.3:p.Gln304=
ENST00000357596.7:c.793C= ENSP00000350209.3:p.Gln265=
ENST00000378319.7:c.910C= ENSP00000367570.3:p.Gln304=
ENST00000426879.5:c.774C=
ENST00000465045.5:c.*277C= ENSP00000418630.1:n.*277C=
ENST00000486276.1:n.339C=
ENST00000488958.5:c.793C= ENSP00000417539.1:p.Gln265=
ENST00000621822.4:c.*218C= ENSP00000482432.1:n.*218C=
NM_001040443.1:c.910C= NP_001035533.1:p.Gln304=
NM_001040444.1:c.793C= NP_001035534.1:p.Gln265=
XM_005266417.2:c.424C= XP_005266474.1:p.Gln142=
XM_006719829.1:c.793C= XP_006719892.1:p.Gln265=
XM_006719830.1:c.793C= XP_006719893.1:p.Gln265=
XM_011535102.1:c.793C= XP_011533404.1:p.Gln265=
XR_941597.1:n.1234C=
NM_001040443.2:c.910C= NP_001035533.1:p.Gln304=
NM_001040444.2:c.793C= NP_001035534.1:p.Gln265=
NM_001320727.1:c.2392C= NP_001307656.1:p.Gln798=
NR_135322.1:n.1180C=
NR_135323.1:n.1279C=
NR_135324.1:n.3502C=
NM_001040443.3:c.910C= MANE Select NP_001035533.1:p.Gln304=
NM_001320727.2:c.2392C= NP_001307656.1:p.Gln798=
NR_135322.2:n.837C=
NR_135323.2:n.1229C=
NR_135324.2:n.3521C=