Canonical Allele Identifier: CA414712792

Gene: PHF6

Linked Data

• MyVariant Identifiers: chrX:g.133547868C>G (hg19) ; chrX:g.134413838C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.134413838C>G , CM000685.2:g.134413838C>G	GRCh38
NC_000023.10:g.133547868C>G , CM000685.1:g.133547868C>G	GRCh37
NC_000023.9:g.133375534C>G	NCBI36
NG_008886.1:g.45527C>G , LRG_629:g.45527C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685553.1:c.*520C>G	ENSP00000510193.1:n.*520C>G
ENST00000687496.1:c.499C>G	ENSP00000509551.1:p.His167Asp
ENST00000688598.1:c.499C>G	ENSP00000510410.1:p.His167Asp
ENST00000691812.1:c.601C>G	ENSP00000510211.1:p.His201Asp
ENST00000693759.1:c.*213C>G	ENSP00000509518.1:n.*213C>G
ENST00000370803.8:c.601C>G MANE Select	ENSP00000359839.4:p.His201Asp
ENST00000332070.7:c.601C>G	ENSP00000329097.3:p.His201Asp
ENST00000370799.5:c.604C>G	ENSP00000359835.1:p.His202Asp
ENST00000370800.4:c.604C>G	ENSP00000359836.4:p.His202Asp
ENST00000370803.7:c.601C>G	ENSP00000359839.3:p.His201Asp
ENST00000625464.2:c.604C>G	ENSP00000487420.1:p.His202Asp
NM_001015877.1:c.601C>G , LRG_629t1:c.601C>G	NP_001015877.1:p.His201Asp
NM_032335.3:c.604C>G , LRG_629t2:c.604C>G	NP_115711.2:p.His202Asp
NM_032458.2:c.601C>G	NP_115834.1:p.His201Asp
NM_001015877.2:c.601C>G MANE Select	NP_001015877.1:p.His201Asp
NM_032458.3:c.601C>G	NP_115834.1:p.His201Asp