Canonical Allele Identifier: CA518651058

Gene: PHF6

Linked Data

• MyVariant Identifiers: chrX:g.133547882T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.134413852T>C , CM000685.2:g.134413852T>C	GRCh38
NC_000023.10:g.133547882T>C , CM000685.1:g.133547882T>C	GRCh37
NC_000023.9:g.133375548T>C	NCBI36
NG_008886.1:g.45541T>C , LRG_629:g.45541T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000685553.1:c.*534T>C	ENSP00000510193.1:n.*534T>C
ENST00000687496.1:c.513T>C	ENSP00000509551.1:p.Pro171=
ENST00000688598.1:c.513T>C	ENSP00000510410.1:p.Pro171=
ENST00000691812.1:c.615T>C	ENSP00000510211.1:p.Pro205=
ENST00000693759.1:c.*227T>C	ENSP00000509518.1:n.*227T>C
ENST00000370803.8:c.615T>C MANE Select	ENSP00000359839.4:p.Pro205=
ENST00000332070.7:c.615T>C	ENSP00000329097.3:p.Pro205=
ENST00000370799.5:c.618T>C	ENSP00000359835.1:p.Pro206=
ENST00000370800.4:c.618T>C	ENSP00000359836.4:p.Pro206=
ENST00000370803.7:c.615T>C	ENSP00000359839.3:p.Pro205=
ENST00000625464.2:c.618T>C	ENSP00000487420.1:p.Pro206=
NM_001015877.1:c.615T>C , LRG_629t1:c.615T>C	NP_001015877.1:p.Pro205=
NM_032335.3:c.618T>C , LRG_629t2:c.618T>C	NP_115711.2:p.Pro206=
NM_032458.2:c.615T>C	NP_115834.1:p.Pro205=
NM_001015877.2:c.615T>C MANE Select	NP_001015877.1:p.Pro205=
NM_032458.3:c.615T>C	NP_115834.1:p.Pro205=