Canonical Allele Identifier: CA412574293
Community Standard Title: NM_000444.6(PHEX):c.1971C>G (p.Tyr657Ter)
Gene: PHEX HGNC NCBI
PTCHD1-AS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22227512C>G , CM000685.2:g.22227512C>G GRCh38
NC_000023.10:g.22245629C>G , CM000685.1:g.22245629C>G GRCh37
NC_000023.9:g.22155550C>G NCBI36
NG_007563.2:g.199709C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000444.6:c.1971C>G (PHEX) MANE Select NP_000435.3:p.Tyr657Ter
ENST00000379374.5:c.1971C>G (PHEX) MANE Select ENSP00000368682.4:p.Tyr657Ter
NM_000444.5:c.1971C>G (PHEX) NP_000435.3:p.Tyr657Ter
NM_001282754.1:c.1971C>G (PHEX) NP_001269683.1:p.Tyr657Ter
NM_001282754.2:c.1971C>G (PHEX) NP_001269683.1:p.Tyr657Ter
NR_073010.2:n.1006G>C (PTCHD1-AS)
ENST00000379374.4:c.1971C>G (PHEX) ENSP00000368682.4:p.Tyr657Ter
ENST00000683162.1:c.525C>G (PHEX) ENSP00000508059.1:p.Tyr175Ter
ENST00000683289.1:c.525C>G (PHEX) ENSP00000508195.1:p.Tyr175Ter
ENST00000683917.1:n.755C>G (PHEX)
ENST00000684356.1:c.525C>G (PHEX) ENSP00000507619.1:p.Tyr175Ter
ENST00000684745.1:n.1645C>G (PHEX)
XM_011545533.1:c.1215C>G (PHEX) XP_011543835.1:p.Tyr405Ter
XM_011545534.1:c.1215C>G (PHEX) XP_011543836.1:p.Tyr405Ter
XM_011545536.1:c.864C>G (PHEX) XP_011543838.1:p.Tyr288Ter
XM_011545536.2:c.864C>G (PHEX) XP_011543838.1:p.Tyr288Ter
XM_017029579.1:c.1215C>G (PHEX) XP_016885068.1:p.Tyr405Ter
XM_024452390.1:c.1680C>G (PHEX) XP_024308158.1:p.Tyr560Ter
XR_001755695.1:n.2811C>G (PHEX)
XR_950534.1:n.283G>C