Canonical Allele Identifier: CA2419152377
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22047150A= , CM000685.2:g.22047150A= GRCh38
NC_000023.10:g.22065268A= , CM000685.1:g.22065268A= GRCh37
NC_000023.9:g.21975189A= NCBI36
NG_007563.2:g.19348A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000475778.2:n.714A=
ENST00000683214.1:n.544+14027A=
ENST00000684143.1:c.288A= ENSP00000508264.1:p.Glu96=
ENST00000379374.5:c.288A= MANE Select ENSP00000368682.4:p.Glu96=
ENST00000379374.4:c.288A= ENSP00000368682.4:p.Glu96=
NM_000444.5:c.288A= NP_000435.3:p.Glu96=
NM_001282754.1:c.288A= NP_001269683.1:p.Glu96=
XM_011545535.1:c.288A= XP_011543837.1:p.Glu96=
XM_024452390.1:c.-4A= XP_024308158.1:n.-4A=
XR_001755695.1:n.967A=
NM_000444.6:c.288A= MANE Select NP_000435.3:p.Glu96=
NM_001282754.2:c.288A= NP_001269683.1:p.Glu96=