Canonical Allele Identifier: CA2419181307
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22133534G= , CM000685.2:g.22133534G= GRCh38
NC_000023.10:g.22151651G= , CM000685.1:g.22151651G= GRCh37
NC_000023.9:g.22061572G= NCBI36
NG_007563.2:g.105731G=

Transcript Alleles

HGVS Amino-acid change
ENST00000684745.1:n.988G=
ENST00000379374.5:c.1314G= MANE Select ENSP00000368682.4:p.Leu438=
ENST00000379374.4:c.1314G= ENSP00000368682.4:p.Leu438=
NM_000444.5:c.1314G= NP_000435.3:p.Leu438=
NM_001282754.1:c.1314G= NP_001269683.1:p.Leu438=
XM_011545533.1:c.558G= XP_011543835.1:p.Leu186=
XM_011545534.1:c.558G= XP_011543836.1:p.Leu186=
XM_011545535.1:c.1314G= XP_011543837.1:p.Leu438=
XM_011545536.1:c.207G= XP_011543838.1:p.Leu69=
XM_011545536.2:c.207G= XP_011543838.1:p.Leu69=
XM_017029579.1:c.558G= XP_016885068.1:p.Leu186=
XM_024452390.1:c.1023G= XP_024308158.1:p.Leu341=
XR_001755695.1:n.1993G=
NM_000444.6:c.1314G= MANE Select NP_000435.3:p.Leu438=
NM_001282754.2:c.1314G= NP_001269683.1:p.Leu438=