Canonical Allele Identifier: CA412567582
Gene: PHEX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22047094G>A , CM000685.2:g.22047094G>A GRCh38
NC_000023.10:g.22065212G>A , CM000685.1:g.22065212G>A GRCh37
NC_000023.9:g.21975133G>A NCBI36
NG_007563.2:g.19292G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000475778.2:n.658G>A
ENST00000683214.1:n.544+13971G>A
ENST00000684143.1:c.232G>A ENSP00000508264.1:p.Asp78Asn
ENST00000379374.5:c.232G>A MANE Select ENSP00000368682.4:p.Asp78Asn
ENST00000379374.4:c.232G>A ENSP00000368682.4:p.Asp78Asn
NM_000444.5:c.232G>A NP_000435.3:p.Asp78Asn
NM_001282754.1:c.232G>A NP_001269683.1:p.Asp78Asn
XM_011545535.1:c.232G>A XP_011543837.1:p.Asp78Asn
XM_024452390.1:c.-60G>A XP_024308158.1:n.-60G>A
XR_001755695.1:n.911G>A
NM_000444.6:c.232G>A MANE Select NP_000435.3:p.Asp78Asn
NM_001282754.2:c.232G>A NP_001269683.1:p.Asp78Asn