Canonical Allele Identifier: CA2419168571
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22096932T= , CM000685.2:g.22096932T= GRCh38
NC_000023.10:g.22115050T= , CM000685.1:g.22115050T= GRCh37
NC_000023.9:g.22024971T= NCBI36
NG_007563.2:g.69130T=

Transcript Alleles

HGVS Amino-acid change
ENST00000475778.2:n.1276-23T=
ENST00000684143.1:c.847-23T= ENSP00000508264.1:n.847-23T=
ENST00000684745.1:n.524-23T=
ENST00000379374.5:c.850-23T= MANE Select ENSP00000368682.4:n.850-23T=
ENST00000379374.4:c.850-23T= ENSP00000368682.4:n.850-23T=
ENST00000475778.1:n.123-23T=
NM_000444.5:c.850-23T= NP_000435.3:n.850-23T=
NM_001282754.1:c.850-23T= NP_001269683.1:n.850-23T=
XM_011545533.1:c.94-23T= XP_011543835.1:n.94-23T=
XM_011545534.1:c.94-23T= XP_011543836.1:n.94-23T=
XM_011545535.1:c.850-23T= XP_011543837.1:n.850-23T=
XM_017029579.1:c.94-23T= XP_016885068.1:n.94-23T=
XM_024452390.1:c.559-23T= XP_024308158.1:n.559-23T=
XR_001755695.1:n.1529-23T=
NM_000444.6:c.850-23T= MANE Select NP_000435.3:n.850-23T=
NM_001282754.2:c.850-23T= NP_001269683.1:n.850-23T=