Canonical Allele Identifier: CA412567607
Gene: PHEX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22047103T>G , CM000685.2:g.22047103T>G GRCh38
NC_000023.10:g.22065221T>G , CM000685.1:g.22065221T>G GRCh37
NC_000023.9:g.21975142T>G NCBI36
NG_007563.2:g.19301T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000475778.2:n.667T>G
ENST00000683214.1:n.544+13980T>G
ENST00000684143.1:c.241T>G ENSP00000508264.1:p.Phe81Val
ENST00000379374.5:c.241T>G MANE Select ENSP00000368682.4:p.Phe81Val
ENST00000379374.4:c.241T>G ENSP00000368682.4:p.Phe81Val
NM_000444.5:c.241T>G NP_000435.3:p.Phe81Val
NM_001282754.1:c.241T>G NP_001269683.1:p.Phe81Val
XM_011545535.1:c.241T>G XP_011543837.1:p.Phe81Val
XM_024452390.1:c.-51T>G XP_024308158.1:n.-51T>G
XR_001755695.1:n.920T>G
NM_000444.6:c.241T>G MANE Select NP_000435.3:p.Phe81Val
NM_001282754.2:c.241T>G NP_001269683.1:p.Phe81Val