Canonical Allele Identifier: CA412574150
Gene: PHEX HGNC NCBI
PTCHD1-AS HGNC NCBI

Linked Data

gnomAD v4: X-22226454-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22226454G>T , CM000685.2:g.22226454G>T GRCh38
NC_000023.10:g.22244571G>T , CM000685.1:g.22244571G>T GRCh37
NC_000023.9:g.22154492G>T NCBI36
NG_007563.2:g.198651G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682888.1:c.465G>T (PHEX) ENSP00000508003.1:p.Lys155Asn
ENST00000683162.1:c.465G>T (PHEX) ENSP00000508059.1:p.Lys155Asn
ENST00000683289.1:c.465G>T (PHEX) ENSP00000508195.1:p.Lys155Asn
ENST00000683917.1:n.695G>T (PHEX)
ENST00000684356.1:c.465G>T (PHEX) ENSP00000507619.1:p.Lys155Asn
ENST00000684745.1:n.1585G>T (PHEX)
ENST00000379374.5:c.1911G>T (PHEX) MANE Select ENSP00000368682.4:p.Lys637Asn
ENST00000379374.4:c.1911G>T (PHEX) ENSP00000368682.4:p.Lys637Asn
NM_000444.5:c.1911G>T (PHEX) NP_000435.3:p.Lys637Asn
NM_001282754.1:c.1911G>T (PHEX) NP_001269683.1:p.Lys637Asn
XM_011545533.1:c.1155G>T (PHEX) XP_011543835.1:p.Lys385Asn
XM_011545534.1:c.1155G>T (PHEX) XP_011543836.1:p.Lys385Asn
XM_011545536.1:c.804G>T (PHEX) XP_011543838.1:p.Lys268Asn
XR_950534.1:n.326-431C>A
NR_073010.2:n.1048+1016C>A (PTCHD1-AS)
XM_011545536.2:c.804G>T (PHEX) XP_011543838.1:p.Lys268Asn
XM_017029579.1:c.1155G>T (PHEX) XP_016885068.1:p.Lys385Asn
XM_024452390.1:c.1620G>T (PHEX) XP_024308158.1:p.Lys540Asn
XR_001755695.1:n.2751G>T (PHEX)
NM_000444.6:c.1911G>T (PHEX) MANE Select NP_000435.3:p.Lys637Asn
NM_001282754.2:c.1911G>T (PHEX) NP_001269683.1:p.Lys637Asn