Canonical Allele Identifier: CA2554421612
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22046756G>A , CM000685.2:g.22046756G>A GRCh38
NC_000023.10:g.22064874G>A , CM000685.1:g.22064874G>A GRCh37
NC_000023.9:g.21974795G>A NCBI36
NG_007563.2:g.18954G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000475778.2:n.614-294G>A
ENST00000683214.1:n.544+13633G>A
ENST00000684143.1:c.188-294G>A ENSP00000508264.1:n.188-294G>A
ENST00000379374.5:c.188-294G>A MANE Select ENSP00000368682.4:n.188-294G>A
ENST00000379374.4:c.188-294G>A ENSP00000368682.4:n.188-294G>A
NM_000444.5:c.188-294G>A NP_000435.3:n.188-294G>A
NM_001282754.1:c.188-294G>A NP_001269683.1:n.188-294G>A
XM_011545535.1:c.188-294G>A XP_011543837.1:n.188-294G>A
XM_024452390.1:c.-104-294G>A XP_024308158.1:n.-104-294G>A
XR_001755695.1:n.867-294G>A
NM_000444.6:c.188-294G>A MANE Select NP_000435.3:n.188-294G>A
NM_001282754.2:c.188-294G>A NP_001269683.1:n.188-294G>A