Canonical Allele Identifier: CA412563708
Gene: PHEX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22033015G>T , CM000685.2:g.22033015G>T GRCh38
NC_000023.10:g.22051133G>T , CM000685.1:g.22051133G>T GRCh37
NC_000023.9:g.21961054G>T NCBI36
NG_007563.2:g.5213G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000475778.2:n.436G>T
ENST00000683214.1:n.436G>T
ENST00000684143.1:c.10G>T ENSP00000508264.1:p.Glu4Ter
ENST00000379374.5:c.10G>T MANE Select ENSP00000368682.4:p.Glu4Ter
ENST00000379374.4:c.10G>T ENSP00000368682.4:p.Glu4Ter
NM_000444.5:c.10G>T NP_000435.3:p.Glu4Ter
NM_001282754.1:c.10G>T NP_001269683.1:p.Glu4Ter
XM_011545535.1:c.10G>T XP_011543837.1:p.Glu4Ter
XR_001755695.1:n.689G>T
NM_000444.6:c.10G>T MANE Select NP_000435.3:p.Glu4Ter
NM_001282754.2:c.10G>T NP_001269683.1:p.Glu4Ter