Canonical Allele Identifier: CA412574837
Gene: PHEX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22178299T>G , CM000685.2:g.22178299T>G GRCh38
NC_000023.10:g.22196416T>G , CM000685.1:g.22196416T>G GRCh37
NC_000023.9:g.22106337T>G NCBI36
NG_007563.2:g.150496T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682888.1:c.63T>G ENSP00000508003.1:p.Phe21Leu
ENST00000683162.1:c.63T>G ENSP00000508059.1:p.Phe21Leu
ENST00000683289.1:c.63T>G ENSP00000508195.1:p.Phe21Leu
ENST00000683917.1:n.293T>G
ENST00000684356.1:c.63T>G ENSP00000507619.1:p.Phe21Leu
ENST00000684745.1:n.1183T>G
ENST00000379374.5:c.1509T>G MANE Select ENSP00000368682.4:p.Phe503Leu
ENST00000379374.4:c.1509T>G ENSP00000368682.4:p.Phe503Leu
NM_000444.5:c.1509T>G NP_000435.3:p.Phe503Leu
NM_001282754.1:c.1509T>G NP_001269683.1:p.Phe503Leu
XM_011545533.1:c.753T>G XP_011543835.1:p.Phe251Leu
XM_011545534.1:c.753T>G XP_011543836.1:p.Phe251Leu
XM_011545536.1:c.402T>G XP_011543838.1:p.Phe134Leu
XM_011545536.2:c.402T>G XP_011543838.1:p.Phe134Leu
XM_017029579.1:c.753T>G XP_016885068.1:p.Phe251Leu
XM_024452390.1:c.1218T>G XP_024308158.1:p.Phe406Leu
XR_001755695.1:n.2349T>G
NM_000444.6:c.1509T>G MANE Select NP_000435.3:p.Phe503Leu
NM_001282754.2:c.1509T>G NP_001269683.1:p.Phe503Leu