Canonical Allele Identifier: CA2419152407
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22047246T= , CM000685.2:g.22047246T= GRCh38
NC_000023.10:g.22065364T= , CM000685.1:g.22065364T= GRCh37
NC_000023.9:g.21975285T= NCBI36
NG_007563.2:g.19444T=

Transcript Alleles

HGVS Amino-acid change
ENST00000475778.2:n.775+35T=
ENST00000683214.1:n.544+14123T=
ENST00000684143.1:c.349+35T= ENSP00000508264.1:n.349+35T=
ENST00000379374.5:c.349+35T= MANE Select ENSP00000368682.4:n.349+35T=
ENST00000379374.4:c.349+35T= ENSP00000368682.4:n.349+35T=
NM_000444.5:c.349+35T= NP_000435.3:n.349+35T=
NM_001282754.1:c.349+35T= NP_001269683.1:n.349+35T=
XM_011545535.1:c.349+35T= XP_011543837.1:n.349+35T=
XM_017029579.1:c.-94+35T= XP_016885068.1:n.-94+35T=
XM_024452390.1:c.58+35T= XP_024308158.1:n.58+35T=
XR_001755695.1:n.1028+35T=
NM_000444.6:c.349+35T= MANE Select NP_000435.3:n.349+35T=
NM_001282754.2:c.349+35T= NP_001269683.1:n.349+35T=