Canonical Allele Identifier: CA518651927

Gene: PHF6

Linked Data

• MyVariant Identifiers: chrX:g.133549105T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.134415075T>C , CM000685.2:g.134415075T>C	GRCh38
NC_000023.10:g.133549105T>C , CM000685.1:g.133549105T>C	GRCh37
NC_000023.9:g.133376771T>C	NCBI36
NG_008886.1:g.46764T>C , LRG_629:g.46764T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685553.1:c.*708T>C	ENSP00000510193.1:n.*708T>C
ENST00000687496.1:c.687T>C	ENSP00000509551.1:p.Phe229=
ENST00000688598.1:c.687T>C	ENSP00000510410.1:p.Phe229=
ENST00000691812.1:c.789T>C	ENSP00000510211.1:p.Phe263=
ENST00000693759.1:c.*401T>C	ENSP00000509518.1:n.*401T>C
ENST00000370803.8:c.789T>C MANE Select	ENSP00000359839.4:p.Phe263=
ENST00000332070.7:c.789T>C	ENSP00000329097.3:p.Phe263=
ENST00000370799.5:c.792T>C	ENSP00000359835.1:p.Phe264=
ENST00000370800.4:c.792T>C	ENSP00000359836.4:p.Phe264=
ENST00000370803.7:c.789T>C	ENSP00000359839.3:p.Phe263=
ENST00000625464.2:c.792T>C	ENSP00000487420.1:p.Phe264=
NM_001015877.1:c.789T>C , LRG_629t1:c.789T>C	NP_001015877.1:p.Phe263=
NM_032335.3:c.792T>C , LRG_629t2:c.792T>C	NP_115711.2:p.Phe264=
NM_032458.2:c.789T>C	NP_115834.1:p.Phe263=
NM_001015877.2:c.789T>C MANE Select	NP_001015877.1:p.Phe263=
NM_032458.3:c.789T>C	NP_115834.1:p.Phe263=