Canonical Allele Identifier: CA2693308494

Gene: PHEX PTCHD1-AS

Linked Data

• gnomAD v4: X-22247996-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22247996C>T , CM000685.2:g.22247996C>T	GRCh38
NC_000023.10:g.22266113C>T , CM000685.1:g.22266113C>T	GRCh37
NC_000023.9:g.22176034C>T	NCBI36
NG_007563.2:g.220193C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683162.1:c.*231C>T (PHEX)	ENSP00000508059.1:n.*231C>T
ENST00000683289.1:c.624+20385C>T (PHEX)	ENSP00000508195.1:n.624+20385C>T
ENST00000683917.1:n.1077C>T (PHEX)
ENST00000684356.1:c.*43C>T (PHEX)	ENSP00000507619.1:n.*43C>T
ENST00000684745.1:n.1967C>T (PHEX)
ENST00000379374.5:c.*43C>T (PHEX) MANE Select	ENSP00000368682.4:n.*43C>T
ENST00000379374.4:c.*43C>T (PHEX)	ENSP00000368682.4:n.*43C>T
NM_000444.5:c.*43C>T (PHEX)	NP_000435.3:n.*43C>T
NM_001282754.1:c.*128C>T (PHEX)	NP_001269683.1:n.*128C>T
XM_011545533.1:c.*43C>T (PHEX)	XP_011543835.1:n.*43C>T
XM_011545534.1:c.*43C>T (PHEX)	XP_011543836.1:n.*43C>T
XM_011545536.1:c.*43C>T (PHEX)	XP_011543838.1:n.*43C>T
XR_950533.1:n.140+5943G>A
XR_950534.1:n.127+5943G>A
NR_073010.2:n.850+5943G>A (PTCHD1-AS)
XM_011545536.2:c.*43C>T (PHEX)	XP_011543838.1:n.*43C>T
XM_017029579.1:c.*43C>T (PHEX)	XP_016885068.1:n.*43C>T
XM_024452390.1:c.*43C>T (PHEX)	XP_024308158.1:n.*43C>T
XR_001755695.1:n.3133C>T (PHEX)
NM_000444.6:c.*43C>T (PHEX) MANE Select	NP_000435.3:n.*43C>T
NM_001282754.2:c.*128C>T (PHEX)	NP_001269683.1:n.*128C>T