Canonical Allele Identifier: CA2419152383
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22047161G= , CM000685.2:g.22047161G= GRCh38
NC_000023.10:g.22065279G= , CM000685.1:g.22065279G= GRCh37
NC_000023.9:g.21975200G= NCBI36
NG_007563.2:g.19359G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000475778.2:n.725G=
ENST00000683214.1:n.544+14038G=
ENST00000684143.1:c.299G= ENSP00000508264.1:p.Ser100=
ENST00000379374.5:c.299G= MANE Select ENSP00000368682.4:p.Ser100=
ENST00000379374.4:c.299G= ENSP00000368682.4:p.Ser100=
NM_000444.5:c.299G= NP_000435.3:p.Ser100=
NM_001282754.1:c.299G= NP_001269683.1:p.Ser100=
XM_011545535.1:c.299G= XP_011543837.1:p.Ser100=
XM_024452390.1:c.8G= XP_024308158.1:p.Ser3=
XR_001755695.1:n.978G=
NM_000444.6:c.299G= MANE Select NP_000435.3:p.Ser100=
NM_001282754.2:c.299G= NP_001269683.1:p.Ser100=