Canonical Allele Identifier: CA412572565

Gene: PHEX

Linked Data

• MyVariant Identifiers: chrX:g.22115089A>C (hg19) ; chrX:g.22096971A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22096971A>C , CM000685.2:g.22096971A>C	GRCh38
NC_000023.10:g.22115089A>C , CM000685.1:g.22115089A>C	GRCh37
NC_000023.9:g.22025010A>C	NCBI36
NG_007563.2:g.69169A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.1292A>C
ENST00000684143.1:c.863A>C	ENSP00000508264.1:p.Glu288Ala
ENST00000684745.1:n.540A>C
ENST00000379374.5:c.866A>C MANE Select	ENSP00000368682.4:p.Glu289Ala
ENST00000379374.4:c.866A>C	ENSP00000368682.4:p.Glu289Ala
ENST00000475778.1:n.139A>C
NM_000444.5:c.866A>C	NP_000435.3:p.Glu289Ala
NM_001282754.1:c.866A>C	NP_001269683.1:p.Glu289Ala
XM_011545533.1:c.110A>C	XP_011543835.1:p.Glu37Ala
XM_011545534.1:c.110A>C	XP_011543836.1:p.Glu37Ala
XM_011545535.1:c.866A>C	XP_011543837.1:p.Glu289Ala
XM_017029579.1:c.110A>C	XP_016885068.1:p.Glu37Ala
XM_024452390.1:c.575A>C	XP_024308158.1:p.Glu192Ala
XR_001755695.1:n.1545A>C
NM_000444.6:c.866A>C MANE Select	NP_000435.3:p.Glu289Ala
NM_001282754.2:c.866A>C	NP_001269683.1:p.Glu289Ala