Canonical Allele Identifier: CA2419161932
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22076370C= , CM000685.2:g.22076370C= GRCh38
NC_000023.10:g.22094488C= , CM000685.1:g.22094488C= GRCh37
NC_000023.9:g.22004409C= NCBI36
NG_007563.2:g.48568C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000475778.2:n.776-18C=
ENST00000683214.1:n.545-1106C=
ENST00000684143.1:c.350-18C= ENSP00000508264.1:n.350-18C=
ENST00000684745.1:n.27-18C=
ENST00000379374.5:c.350-18C= MANE Select ENSP00000368682.4:n.350-18C=
ENST00000379374.4:c.350-18C= ENSP00000368682.4:n.350-18C=
NM_000444.5:c.350-18C= NP_000435.3:n.350-18C=
NM_001282754.1:c.350-18C= NP_001269683.1:n.350-18C=
XM_011545535.1:c.350-18C= XP_011543837.1:n.350-18C=
XM_017029579.1:c.-93-14059C= XP_016885068.1:n.-93-14059C=
XM_024452390.1:c.59-18C= XP_024308158.1:n.59-18C=
XR_001755695.1:n.1029-18C=
NM_000444.6:c.350-18C= MANE Select NP_000435.3:n.350-18C=
NM_001282754.2:c.350-18C= NP_001269683.1:n.350-18C=