Canonical Allele Identifier: CA2419195567
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22178285G= , CM000685.2:g.22178285G= GRCh38
NC_000023.10:g.22196402G= , CM000685.1:g.22196402G= GRCh37
NC_000023.9:g.22106323G= NCBI36
NG_007563.2:g.150482G=

Transcript Alleles

HGVS Amino-acid change
ENST00000682888.1:c.49G= ENSP00000508003.1:p.Glu17=
ENST00000683162.1:c.49G= ENSP00000508059.1:p.Glu17=
ENST00000683289.1:c.49G= ENSP00000508195.1:p.Glu17=
ENST00000683917.1:n.279G=
ENST00000684356.1:c.49G= ENSP00000507619.1:p.Glu17=
ENST00000684745.1:n.1169G=
ENST00000379374.5:c.1495G= MANE Select ENSP00000368682.4:p.Glu499=
ENST00000379374.4:c.1495G= ENSP00000368682.4:p.Glu499=
NM_000444.5:c.1495G= NP_000435.3:p.Glu499=
NM_001282754.1:c.1495G= NP_001269683.1:p.Glu499=
XM_011545533.1:c.739G= XP_011543835.1:p.Glu247=
XM_011545534.1:c.739G= XP_011543836.1:p.Glu247=
XM_011545536.1:c.388G= XP_011543838.1:p.Glu130=
XM_011545536.2:c.388G= XP_011543838.1:p.Glu130=
XM_017029579.1:c.739G= XP_016885068.1:p.Glu247=
XM_024452390.1:c.1204G= XP_024308158.1:p.Glu402=
XR_001755695.1:n.2335G=
NM_000444.6:c.1495G= MANE Select NP_000435.3:p.Glu499=
NM_001282754.2:c.1495G= NP_001269683.1:p.Glu499=