Canonical Allele Identifier: CA412567786
Gene: PHEX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22047182T>A , CM000685.2:g.22047182T>A GRCh38
NC_000023.10:g.22065300T>A , CM000685.1:g.22065300T>A GRCh37
NC_000023.9:g.21975221T>A NCBI36
NG_007563.2:g.19380T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000475778.2:n.746T>A
ENST00000683214.1:n.544+14059T>A
ENST00000684143.1:c.320T>A ENSP00000508264.1:p.Leu107Gln
ENST00000379374.5:c.320T>A MANE Select ENSP00000368682.4:p.Leu107Gln
ENST00000379374.4:c.320T>A ENSP00000368682.4:p.Leu107Gln
NM_000444.5:c.320T>A NP_000435.3:p.Leu107Gln
NM_001282754.1:c.320T>A NP_001269683.1:p.Leu107Gln
XM_011545535.1:c.320T>A XP_011543837.1:p.Leu107Gln
XM_017029579.1:c.-123T>A XP_016885068.1:n.-123T>A
XM_024452390.1:c.29T>A XP_024308158.1:p.Leu10Gln
XR_001755695.1:n.999T>A
NM_000444.6:c.320T>A MANE Select NP_000435.3:p.Leu107Gln
NM_001282754.2:c.320T>A NP_001269683.1:p.Leu107Gln