Canonical Allele Identifier: CA412568064

Gene: PHEX

Linked Data

• MyVariant Identifiers: chrX:g.22065307T>A (hg19) ; chrX:g.22047189T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22047189T>A , CM000685.2:g.22047189T>A	GRCh38
NC_000023.10:g.22065307T>A , CM000685.1:g.22065307T>A	GRCh37
NC_000023.9:g.21975228T>A	NCBI36
NG_007563.2:g.19387T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000475778.2:n.753T>A
ENST00000683214.1:n.544+14066T>A
ENST00000684143.1:c.327T>A	ENSP00000508264.1:p.His109Gln
ENST00000379374.5:c.327T>A MANE Select	ENSP00000368682.4:p.His109Gln
ENST00000379374.4:c.327T>A	ENSP00000368682.4:p.His109Gln
NM_000444.5:c.327T>A	NP_000435.3:p.His109Gln
NM_001282754.1:c.327T>A	NP_001269683.1:p.His109Gln
XM_011545535.1:c.327T>A	XP_011543837.1:p.His109Gln
XM_017029579.1:c.-116T>A	XP_016885068.1:n.-116T>A
XM_024452390.1:c.36T>A	XP_024308158.1:p.His12Gln
XR_001755695.1:n.1006T>A
NM_000444.6:c.327T>A MANE Select	NP_000435.3:p.His109Gln
NM_001282754.2:c.327T>A	NP_001269683.1:p.His109Gln