Canonical Allele Identifier: CA2090489307

Gene: PHF11

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.49528674G= , CM000675.2:g.49528674G=	GRCh38
NC_000013.10:g.50102810G= , CM000675.1:g.50102810G=	GRCh37
NC_000013.9:g.49000811G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001040443.3:c.*9G= MANE Select	NP_001035533.1:n.*9G=
ENST00000378319.8:c.*9G= MANE Select	ENSP00000367570.3:n.*9G=
NM_001040443.1:c.*9G=	NP_001035533.1:n.*9G=
NM_001040443.2:c.*9G=	NP_001035533.1:n.*9G=
NM_001040444.1:c.*9G=	NP_001035534.1:n.*9G=
NM_001040444.2:c.*9G=	NP_001035534.1:n.*9G=
NM_001320727.1:c.*9G=	NP_001307656.1:n.*9G=
NM_001320727.2:c.*9G=	NP_001307656.1:n.*9G=
NR_135322.1:n.1275G=
NR_135322.2:n.932G=
NR_135323.1:n.1374G=
NR_135323.2:n.1324G=
NR_135324.1:n.3597G=
NR_135324.2:n.3616G=
ENST00000357596.7:c.*9G=	ENSP00000350209.3:n.*9G=
ENST00000378319.7:c.*9G=	ENSP00000367570.3:n.*9G=
ENST00000426879.5:c.869G=
ENST00000465045.5:c.*372G=	ENSP00000418630.1:n.*372G=
ENST00000486276.1:n.434G=
ENST00000488958.5:c.*9G=	ENSP00000417539.1:n.*9G=
ENST00000621822.4:c.*313G=	ENSP00000482432.1:n.*313G=
XM_005266417.2:c.*9G=	XP_005266474.1:n.*9G=
XM_006719829.1:c.*9G=	XP_006719892.1:n.*9G=
XM_006719830.1:c.*9G=	XP_006719893.1:n.*9G=
XM_011535102.1:c.*9G=	XP_011533404.1:n.*9G=
XR_941597.1:n.1329G=