Canonical Allele Identifier: CA515429457
Gene: PHEX HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.22095670A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22077552A>G , CM000685.2:g.22077552A>G GRCh38
NC_000023.10:g.22095670A>G , CM000685.1:g.22095670A>G GRCh37
NC_000023.9:g.22005591A>G NCBI36
NG_007563.2:g.49750A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000475778.2:n.939A>G
ENST00000683214.1:n.621A>G
ENST00000684143.1:c.510A>G ENSP00000508264.1:p.Glu170=
ENST00000684745.1:n.187A>G
ENST00000379374.5:c.513A>G MANE Select ENSP00000368682.4:p.Glu171=
ENST00000379374.4:c.513A>G ENSP00000368682.4:p.Glu171=
NM_000444.5:c.513A>G NP_000435.3:p.Glu171=
NM_001282754.1:c.513A>G NP_001269683.1:p.Glu171=
XM_011545535.1:c.513A>G XP_011543837.1:p.Glu171=
XM_017029579.1:c.-93-12877A>G XP_016885068.1:n.-93-12877A>G
XM_024452390.1:c.222A>G XP_024308158.1:p.Glu74=
XR_001755695.1:n.1192A>G
NM_000444.6:c.513A>G MANE Select NP_000435.3:p.Glu171=
NM_001282754.2:c.513A>G NP_001269683.1:p.Glu171=