Canonical Allele Identifier: CA414713212

Gene: PHF6

Linked Data

• MyVariant Identifiers: chrX:g.133549094T>G (hg19) ; chrX:g.134415064T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.134415064T>G , CM000685.2:g.134415064T>G	GRCh38
NC_000023.10:g.133549094T>G , CM000685.1:g.133549094T>G	GRCh37
NC_000023.9:g.133376760T>G	NCBI36
NG_008886.1:g.46753T>G , LRG_629:g.46753T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685553.1:c.*697T>G	ENSP00000510193.1:n.*697T>G
ENST00000687496.1:c.676T>G	ENSP00000509551.1:p.Phe226Val
ENST00000688598.1:c.676T>G	ENSP00000510410.1:p.Phe226Val
ENST00000691812.1:c.778T>G	ENSP00000510211.1:p.Phe260Val
ENST00000693759.1:c.*390T>G	ENSP00000509518.1:n.*390T>G
ENST00000370803.8:c.778T>G MANE Select	ENSP00000359839.4:p.Phe260Val
ENST00000332070.7:c.778T>G	ENSP00000329097.3:p.Phe260Val
ENST00000370799.5:c.781T>G	ENSP00000359835.1:p.Phe261Val
ENST00000370800.4:c.781T>G	ENSP00000359836.4:p.Phe261Val
ENST00000370803.7:c.778T>G	ENSP00000359839.3:p.Phe260Val
ENST00000625464.2:c.781T>G	ENSP00000487420.1:p.Phe261Val
NM_001015877.1:c.778T>G , LRG_629t1:c.778T>G	NP_001015877.1:p.Phe260Val
NM_032335.3:c.781T>G , LRG_629t2:c.781T>G	NP_115711.2:p.Phe261Val
NM_032458.2:c.778T>G	NP_115834.1:p.Phe260Val
NM_001015877.2:c.778T>G MANE Select	NP_001015877.1:p.Phe260Val
NM_032458.3:c.778T>G	NP_115834.1:p.Phe260Val