Canonical Allele Identifier: CA412568058

Gene: PHEX

Linked Data

• dbSNP Id: rs905332203
• MyVariant Identifiers: chrX:g.22065305C>G (hg19) ; chrX:g.22047187C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22047187C>G , CM000685.2:g.22047187C>G	GRCh38
NC_000023.10:g.22065305C>G , CM000685.1:g.22065305C>G	GRCh37
NC_000023.9:g.21975226C>G	NCBI36
NG_007563.2:g.19385C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000475778.2:n.751C>G
ENST00000683214.1:n.544+14064C>G
ENST00000684143.1:c.325C>G	ENSP00000508264.1:p.His109Asp
ENST00000379374.5:c.325C>G MANE Select	ENSP00000368682.4:p.His109Asp
ENST00000379374.4:c.325C>G	ENSP00000368682.4:p.His109Asp
NM_000444.5:c.325C>G	NP_000435.3:p.His109Asp
NM_001282754.1:c.325C>G	NP_001269683.1:p.His109Asp
XM_011545535.1:c.325C>G	XP_011543837.1:p.His109Asp
XM_017029579.1:c.-118C>G	XP_016885068.1:n.-118C>G
XM_024452390.1:c.34C>G	XP_024308158.1:p.His12Asp
XR_001755695.1:n.1004C>G
NM_000444.6:c.325C>G MANE Select	NP_000435.3:p.His109Asp
NM_001282754.2:c.325C>G	NP_001269683.1:p.His109Asp