Canonical Allele Identifier: CA2459705479

Gene: PHF6

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.134377562T= , CM000685.2:g.134377562T=	GRCh38
NC_000023.10:g.133511592T= , CM000685.1:g.133511592T=	GRCh37
NC_000023.9:g.133339258T=	NCBI36
NG_008886.1:g.9251T= , LRG_629:g.9251T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685047.1:c.-46-10T=	ENSP00000509894.1:n.-46-10T=
ENST00000685553.1:c.-46-10T=	ENSP00000510193.1:n.-46-10T=
ENST00000687496.1:c.-46-10T=	ENSP00000509551.1:n.-46-10T=
ENST00000687834.1:n.128-10T=
ENST00000688598.1:c.-46-10T=	ENSP00000510410.1:n.-46-10T=
ENST00000691812.1:c.-46-10T=	ENSP00000510211.1:n.-46-10T=
ENST00000693759.1:c.-46-10T=	ENSP00000509518.1:n.-46-10T=
ENST00000370803.8:c.-46-10T= MANE Select	ENSP00000359839.4:n.-46-10T=
ENST00000332070.7:c.-46-10T=	ENSP00000329097.3:n.-46-10T=
ENST00000370799.5:c.-46-10T=	ENSP00000359835.1:n.-46-10T=
ENST00000370800.4:c.-46-10T=	ENSP00000359836.4:n.-46-10T=
ENST00000370803.7:c.-46-10T=	ENSP00000359839.3:n.-46-10T=
ENST00000625464.2:c.-46-10T=	ENSP00000487420.1:n.-46-10T=
NM_001015877.1:c.-46-10T= , LRG_629t1:c.-46-10T=	NP_001015877.1:n.-46-10T=
NM_032335.3:c.-46-10T= , LRG_629t2:c.-46-10T=	NP_115711.2:n.-46-10T=
NM_032458.2:c.-46-10T=	NP_115834.1:n.-46-10T=
NM_001015877.2:c.-46-10T= MANE Select	NP_001015877.1:n.-46-10T=
NM_032458.3:c.-46-10T=	NP_115834.1:n.-46-10T=