Canonical Allele Identifier: CA515425069
Gene: PHEX HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.22065319C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22047201C>G , CM000685.2:g.22047201C>G GRCh38
NC_000023.10:g.22065319C>G , CM000685.1:g.22065319C>G GRCh37
NC_000023.9:g.21975240C>G NCBI36
NG_007563.2:g.19399C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000475778.2:n.765C>G
ENST00000683214.1:n.544+14078C>G
ENST00000684143.1:c.339C>G ENSP00000508264.1:p.Leu113=
ENST00000379374.5:c.339C>G MANE Select ENSP00000368682.4:p.Leu113=
ENST00000379374.4:c.339C>G ENSP00000368682.4:p.Leu113=
NM_000444.5:c.339C>G NP_000435.3:p.Leu113=
NM_001282754.1:c.339C>G NP_001269683.1:p.Leu113=
XM_011545535.1:c.339C>G XP_011543837.1:p.Leu113=
XM_017029579.1:c.-104C>G XP_016885068.1:n.-104C>G
XM_024452390.1:c.48C>G XP_024308158.1:p.Leu16=
XR_001755695.1:n.1018C>G
NM_000444.6:c.339C>G MANE Select NP_000435.3:p.Leu113=
NM_001282754.2:c.339C>G NP_001269683.1:p.Leu113=