Canonical Allele Identifier: CA2419152391
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22047180G= , CM000685.2:g.22047180G= GRCh38
NC_000023.10:g.22065298G= , CM000685.1:g.22065298G= GRCh37
NC_000023.9:g.21975219G= NCBI36
NG_007563.2:g.19378G=

Transcript Alleles

HGVS Amino-acid change
ENST00000475778.2:n.744G=
ENST00000683214.1:n.544+14057G=
ENST00000684143.1:c.318G= ENSP00000508264.1:p.Trp106=
ENST00000379374.5:c.318G= MANE Select ENSP00000368682.4:p.Trp106=
ENST00000379374.4:c.318G= ENSP00000368682.4:p.Trp106=
NM_000444.5:c.318G= NP_000435.3:p.Trp106=
NM_001282754.1:c.318G= NP_001269683.1:p.Trp106=
XM_011545535.1:c.318G= XP_011543837.1:p.Trp106=
XM_017029579.1:c.-125G= XP_016885068.1:n.-125G=
XM_024452390.1:c.27G= XP_024308158.1:p.Trp9=
XR_001755695.1:n.997G=
NM_000444.6:c.318G= MANE Select NP_000435.3:p.Trp106=
NM_001282754.2:c.318G= NP_001269683.1:p.Trp106=