Canonical Allele Identifier: CA2361819111

Gene: PHF20

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35795692C= , CM000682.2:g.35795692C=	GRCh38
NC_000020.10:g.34383614C= , CM000682.1:g.34383614C=	GRCh37
NC_000020.9:g.33847028C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374012.8:c.-32-5799C= MANE Select	ENSP00000363124.3:n.-32-5799C=
ENST00000339089.10:c.-32-5799C=	ENSP00000341900.6:n.-32-5799C=
ENST00000374000.8:c.-112-4402C=	ENSP00000363112.4:n.-112-4402C=
ENST00000374012.7:c.-32-5799C=	ENSP00000363124.3:n.-32-5799C=
ENST00000452270.5:c.-32-5799C=	ENSP00000404455.1:n.-32-5799C=
ENST00000461122.5:n.106+23613C=
ENST00000461405.1:n.69-5799C=
ENST00000481202.5:n.55-5799C=
NM_016436.4:c.-32-5799C=	NP_057520.2:n.-32-5799C=
XM_011528842.1:c.-32-5799C=	XP_011527144.1:n.-32-5799C=
XM_011528843.1:c.-853-5799C=	XP_011527145.1:n.-853-5799C=
XM_011528845.1:c.-950-5799C=	XP_011527147.1:n.-950-5799C=
XM_011528843.2:c.-853-5799C=	XP_011527145.1:n.-853-5799C=
XM_017027868.2:c.-32-5799C=	XP_016883357.1:n.-32-5799C=
XM_017027869.2:c.-380-4402C=	XP_016883358.1:n.-380-4402C=
XM_017027870.2:c.-397-5799C=	XP_016883359.1:n.-397-5799C=
XM_017027871.2:c.-1338-5799C=	XP_016883360.1:n.-1338-5799C=
XM_024451889.1:c.-300-5799C=	XP_024307657.1:n.-300-5799C=
XM_024451890.1:c.-1606-5799C=	XP_024307658.1:n.-1606-5799C=
NM_016436.5:c.-32-5799C= MANE Select	NP_057520.2:n.-32-5799C=