Canonical Allele Identifier: CA412567587
Gene: PHEX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22047095A>T , CM000685.2:g.22047095A>T GRCh38
NC_000023.10:g.22065213A>T , CM000685.1:g.22065213A>T GRCh37
NC_000023.9:g.21975134A>T NCBI36
NG_007563.2:g.19293A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000475778.2:n.659A>T
ENST00000683214.1:n.544+13972A>T
ENST00000684143.1:c.233A>T ENSP00000508264.1:p.Asp78Val
ENST00000379374.5:c.233A>T MANE Select ENSP00000368682.4:p.Asp78Val
ENST00000379374.4:c.233A>T ENSP00000368682.4:p.Asp78Val
NM_000444.5:c.233A>T NP_000435.3:p.Asp78Val
NM_001282754.1:c.233A>T NP_001269683.1:p.Asp78Val
XM_011545535.1:c.233A>T XP_011543837.1:p.Asp78Val
XM_024452390.1:c.-59A>T XP_024308158.1:n.-59A>T
XR_001755695.1:n.912A>T
NM_000444.6:c.233A>T MANE Select NP_000435.3:p.Asp78Val
NM_001282754.2:c.233A>T NP_001269683.1:p.Asp78Val