Canonical Allele Identifier: CA2419147473
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22032885T= , CM000685.2:g.22032885T= GRCh38
NC_000023.10:g.22051003T= , CM000685.1:g.22051003T= GRCh37
NC_000023.9:g.21960924T= NCBI36
NG_007563.2:g.5083T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000475778.2:n.306T=
ENST00000683214.1:n.306T=
ENST00000684143.1:c.-121T= ENSP00000508264.1:n.-121T=
ENST00000379374.5:c.-121T= MANE Select ENSP00000368682.4:n.-121T=
ENST00000379374.4:c.-121T= ENSP00000368682.4:n.-121T=
NM_000444.5:c.-121T= NP_000435.3:n.-121T=
NM_001282754.1:c.-121T= NP_001269683.1:n.-121T=
XM_011545535.1:c.-121T= XP_011543837.1:n.-121T=
XR_001755695.1:n.559T=
NM_000444.6:c.-121T= MANE Select NP_000435.3:n.-121T=
NM_001282754.2:c.-121T= NP_001269683.1:n.-121T=