Canonical Allele Identifier: CA2459717470

Gene: PHF6

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.134413937A= , CM000685.2:g.134413937A=	GRCh38
NC_000023.10:g.133547967A= , CM000685.1:g.133547967A=	GRCh37
NC_000023.9:g.133375633A=	NCBI36
NG_008886.1:g.45626A= , LRG_629:g.45626A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685553.1:c.*619A=	ENSP00000510193.1:n.*619A=
ENST00000687496.1:c.598A=	ENSP00000509551.1:p.Lys200=
ENST00000688598.1:c.598A=	ENSP00000510410.1:p.Lys200=
ENST00000691812.1:c.700A=	ENSP00000510211.1:p.Lys234=
ENST00000693759.1:c.*312A=	ENSP00000509518.1:n.*312A=
ENST00000370803.8:c.700A= MANE Select	ENSP00000359839.4:p.Lys234=
ENST00000332070.7:c.700A=	ENSP00000329097.3:p.Lys234=
ENST00000370799.5:c.703A=	ENSP00000359835.1:p.Lys235=
ENST00000370800.4:c.703A=	ENSP00000359836.4:p.Lys235=
ENST00000370803.7:c.700A=	ENSP00000359839.3:p.Lys234=
ENST00000625464.2:c.703A=	ENSP00000487420.1:p.Lys235=
NM_001015877.1:c.700A= , LRG_629t1:c.700A=	NP_001015877.1:p.Lys234=
NM_032335.3:c.703A= , LRG_629t2:c.703A=	NP_115711.2:p.Lys235=
NM_032458.2:c.700A=	NP_115834.1:p.Lys234=
NM_001015877.2:c.700A= MANE Select	NP_001015877.1:p.Lys234=
NM_032458.3:c.700A=	NP_115834.1:p.Lys234=