Canonical Allele Identifier: CA412571063

Gene: PHEX

Linked Data

• MyVariant Identifiers: chrX:g.22094525C>G (hg19) ; chrX:g.22076407C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22076407C>G , CM000685.2:g.22076407C>G	GRCh38
NC_000023.10:g.22094525C>G , CM000685.1:g.22094525C>G	GRCh37
NC_000023.9:g.22004446C>G	NCBI36
NG_007563.2:g.48605C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.795C>G
ENST00000683214.1:n.545-1069C>G
ENST00000684143.1:c.369C>G	ENSP00000508264.1:p.Ile123Met
ENST00000684745.1:n.46C>G
ENST00000379374.5:c.369C>G MANE Select	ENSP00000368682.4:p.Ile123Met
ENST00000379374.4:c.369C>G	ENSP00000368682.4:p.Ile123Met
NM_000444.5:c.369C>G	NP_000435.3:p.Ile123Met
NM_001282754.1:c.369C>G	NP_001269683.1:p.Ile123Met
XM_011545535.1:c.369C>G	XP_011543837.1:p.Ile123Met
XM_017029579.1:c.-93-14022C>G	XP_016885068.1:n.-93-14022C>G
XM_024452390.1:c.78C>G	XP_024308158.1:p.Ile26Met
XR_001755695.1:n.1048C>G
NM_000444.6:c.369C>G MANE Select	NP_000435.3:p.Ile123Met
NM_001282754.2:c.369C>G	NP_001269683.1:p.Ile123Met