Canonical Allele Identifier: CA2419167613
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22094009G= , CM000685.2:g.22094009G= GRCh38
NC_000023.10:g.22112127G= , CM000685.1:g.22112127G= GRCh37
NC_000023.9:g.22022048G= NCBI36
NG_007563.2:g.66207G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000475778.2:n.1185G=
ENST00000684143.1:c.756G= ENSP00000508264.1:p.Met252=
ENST00000684745.1:n.433G=
ENST00000379374.5:c.759G= MANE Select ENSP00000368682.4:p.Met253=
ENST00000379374.4:c.759G= ENSP00000368682.4:p.Met253=
ENST00000475778.1:n.32G=
NM_000444.5:c.759G= NP_000435.3:p.Met253=
NM_001282754.1:c.759G= NP_001269683.1:p.Met253=
XM_011545533.1:c.3G= XP_011543835.1:p.Met1=
XM_011545534.1:c.3G= XP_011543836.1:p.Met1=
XM_011545535.1:c.759G= XP_011543837.1:p.Met253=
XM_017029579.1:c.3G= XP_016885068.1:p.Met1=
XM_024452390.1:c.468G= XP_024308158.1:p.Met156=
XR_001755695.1:n.1438G=
NM_000444.6:c.759G= MANE Select NP_000435.3:p.Met253=
NM_001282754.2:c.759G= NP_001269683.1:p.Met253=