Canonical Allele Identifier: CA2579705869

Gene: PHF6

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.134377573A>T , CM000685.2:g.134377573A>T	GRCh38
NC_000023.10:g.133511603A>T , CM000685.1:g.133511603A>T	GRCh37
NC_000023.9:g.133339269A>T	NCBI36
NG_008886.1:g.9262A>T , LRG_629:g.9262A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685047.1:c.-45A>T	ENSP00000509894.1:n.-45A>T
ENST00000685553.1:c.-45A>T	ENSP00000510193.1:n.-45A>T
ENST00000687496.1:c.-45A>T	ENSP00000509551.1:n.-45A>T
ENST00000687834.1:n.129A>T
ENST00000688598.1:c.-45A>T	ENSP00000510410.1:n.-45A>T
ENST00000691812.1:c.-45A>T	ENSP00000510211.1:n.-45A>T
ENST00000693759.1:c.-45A>T	ENSP00000509518.1:n.-45A>T
ENST00000370803.8:c.-45A>T MANE Select	ENSP00000359839.4:n.-45A>T
ENST00000332070.7:c.-45A>T	ENSP00000329097.3:n.-45A>T
ENST00000370799.5:c.-45A>T	ENSP00000359835.1:n.-45A>T
ENST00000370800.4:c.-45A>T	ENSP00000359836.4:n.-45A>T
ENST00000370803.7:c.-45A>T	ENSP00000359839.3:n.-45A>T
ENST00000625464.2:c.-45A>T	ENSP00000487420.1:n.-45A>T
NM_001015877.1:c.-45A>T , LRG_629t1:c.-45A>T	NP_001015877.1:n.-45A>T
NM_032335.3:c.-45A>T , LRG_629t2:c.-45A>T	NP_115711.2:n.-45A>T
NM_032458.2:c.-45A>T	NP_115834.1:n.-45A>T
NM_001015877.2:c.-45A>T MANE Select	NP_001015877.1:n.-45A>T
NM_032458.3:c.-45A>T	NP_115834.1:n.-45A>T