Canonical Allele Identifier: CA2419152328
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22047008T= , CM000685.2:g.22047008T= GRCh38
NC_000023.10:g.22065126T= , CM000685.1:g.22065126T= GRCh37
NC_000023.9:g.21975047T= NCBI36
NG_007563.2:g.19206T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000475778.2:n.614-42T=
ENST00000683214.1:n.544+13885T=
ENST00000684143.1:c.188-42T= ENSP00000508264.1:n.188-42T=
ENST00000379374.5:c.188-42T= MANE Select ENSP00000368682.4:n.188-42T=
ENST00000379374.4:c.188-42T= ENSP00000368682.4:n.188-42T=
NM_000444.5:c.188-42T= NP_000435.3:n.188-42T=
NM_001282754.1:c.188-42T= NP_001269683.1:n.188-42T=
XM_011545535.1:c.188-42T= XP_011543837.1:n.188-42T=
XM_024452390.1:c.-104-42T= XP_024308158.1:n.-104-42T=
XR_001755695.1:n.867-42T=
NM_000444.6:c.188-42T= MANE Select NP_000435.3:n.188-42T=
NM_001282754.2:c.188-42T= NP_001269683.1:n.188-42T=