Canonical Allele Identifier: CA412574387

Gene: PHEX PTCHD1-AS

Linked Data

• MyVariant Identifiers: chrX:g.22245668G>T (hg19) ; chrX:g.22227551G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22227551G>T , CM000685.2:g.22227551G>T	GRCh38
NC_000023.10:g.22245668G>T , CM000685.1:g.22245668G>T	GRCh37
NC_000023.9:g.22155589G>T	NCBI36
NG_007563.2:g.199748G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000683162.1:c.564G>T (PHEX)	ENSP00000508059.1:p.Glu188Asp
ENST00000683289.1:c.564G>T (PHEX)	ENSP00000508195.1:p.Glu188Asp
ENST00000683917.1:n.794G>T (PHEX)
ENST00000684356.1:c.564G>T (PHEX)	ENSP00000507619.1:p.Glu188Asp
ENST00000684745.1:n.1684G>T (PHEX)
ENST00000379374.5:c.2010G>T (PHEX) MANE Select	ENSP00000368682.4:p.Glu670Asp
ENST00000379374.4:c.2010G>T (PHEX)	ENSP00000368682.4:p.Glu670Asp
NM_000444.5:c.2010G>T (PHEX)	NP_000435.3:p.Glu670Asp
NM_001282754.1:c.2010G>T (PHEX)	NP_001269683.1:p.Glu670Asp
XM_011545533.1:c.1254G>T (PHEX)	XP_011543835.1:p.Glu418Asp
XM_011545534.1:c.1254G>T (PHEX)	XP_011543836.1:p.Glu418Asp
XM_011545536.1:c.903G>T (PHEX)	XP_011543838.1:p.Glu301Asp
XR_950534.1:n.244C>A
NR_073010.2:n.967C>A (PTCHD1-AS)
XM_011545536.2:c.903G>T (PHEX)	XP_011543838.1:p.Glu301Asp
XM_017029579.1:c.1254G>T (PHEX)	XP_016885068.1:p.Glu418Asp
XM_024452390.1:c.1719G>T (PHEX)	XP_024308158.1:p.Glu573Asp
XR_001755695.1:n.2850G>T (PHEX)
NM_000444.6:c.2010G>T (PHEX) MANE Select	NP_000435.3:p.Glu670Asp
NM_001282754.2:c.2010G>T (PHEX)	NP_001269683.1:p.Glu670Asp