Canonical Allele Identifier: CA412571408

Gene: PHEX

Linked Data

• MyVariant Identifiers: chrX:g.22095683C>A (hg19) ; chrX:g.22077565C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22077565C>A , CM000685.2:g.22077565C>A	GRCh38
NC_000023.10:g.22095683C>A , CM000685.1:g.22095683C>A	GRCh37
NC_000023.9:g.22005604C>A	NCBI36
NG_007563.2:g.49763C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.952C>A
ENST00000683214.1:n.634C>A
ENST00000684143.1:c.523C>A	ENSP00000508264.1:p.Pro175Thr
ENST00000684745.1:n.200C>A
ENST00000379374.5:c.526C>A MANE Select	ENSP00000368682.4:p.Pro176Thr
ENST00000379374.4:c.526C>A	ENSP00000368682.4:p.Pro176Thr
NM_000444.5:c.526C>A	NP_000435.3:p.Pro176Thr
NM_001282754.1:c.526C>A	NP_001269683.1:p.Pro176Thr
XM_011545535.1:c.526C>A	XP_011543837.1:p.Pro176Thr
XM_017029579.1:c.-93-12864C>A	XP_016885068.1:n.-93-12864C>A
XM_024452390.1:c.235C>A	XP_024308158.1:p.Pro79Thr
XR_001755695.1:n.1205C>A
NM_000444.6:c.526C>A MANE Select	NP_000435.3:p.Pro176Thr
NM_001282754.2:c.526C>A	NP_001269683.1:p.Pro176Thr