Canonical Allele Identifier: CA412572078
Community Standard Title: NM_000444.6(PHEX):c.705C>A (p.Tyr235Ter)
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22090470C>A , CM000685.2:g.22090470C>A GRCh38
NC_000023.10:g.22108588C>A , CM000685.1:g.22108588C>A GRCh37
NC_000023.9:g.22018509C>A NCBI36
NG_007563.2:g.62668C>A

Transcript Alleles

HGVS Amino-acid Change
NM_000444.6:c.705C>A MANE Select NP_000435.3:p.Tyr235Ter
ENST00000379374.5:c.705C>A MANE Select ENSP00000368682.4:p.Tyr235Ter
NM_000444.5:c.705C>A NP_000435.3:p.Tyr235Ter
NM_001282754.1:c.705C>A NP_001269683.1:p.Tyr235Ter
NM_001282754.2:c.705C>A NP_001269683.1:p.Tyr235Ter
ENST00000379374.4:c.705C>A ENSP00000368682.4:p.Tyr235Ter
ENST00000475778.2:n.1131C>A
ENST00000684143.1:c.702C>A ENSP00000508264.1:p.Tyr234Ter
ENST00000684745.1:n.379C>A
XM_011545533.1:c.-52C>A XP_011543835.1:n.-52C>A
XM_011545534.1:c.-52C>A XP_011543836.1:n.-52C>A
XM_011545535.1:c.705C>A XP_011543837.1:p.Tyr235Ter
XM_017029579.1:c.-52C>A XP_016885068.1:n.-52C>A
XM_024452390.1:c.414C>A XP_024308158.1:p.Tyr138Ter
XR_001755695.1:n.1384C>A