Canonical Allele Identifier: CA2820019565

Gene: PHEX PTCHD1-AS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22248219T>C , CM000685.2:g.22248219T>C	GRCh38
NC_000023.10:g.22266336T>C , CM000685.1:g.22266336T>C	GRCh37
NC_000023.9:g.22176257T>C	NCBI36
NG_007563.2:g.220416T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683162.1:c.*454T>C (PHEX)	ENSP00000508059.1:n.*454T>C
ENST00000683289.1:c.624+20608T>C (PHEX)	ENSP00000508195.1:n.624+20608T>C
ENST00000683917.1:n.1158+142T>C (PHEX)
ENST00000684356.1:c.*266T>C (PHEX)	ENSP00000507619.1:n.*266T>C
ENST00000684745.1:n.2190T>C (PHEX)
ENST00000379374.5:c.*266T>C (PHEX) MANE Select	ENSP00000368682.4:n.*266T>C
ENST00000379374.4:c.*266T>C (PHEX)	ENSP00000368682.4:n.*266T>C
NM_000444.5:c.*266T>C (PHEX)	NP_000435.3:n.*266T>C
NM_001282754.1:c.*351T>C (PHEX)	NP_001269683.1:n.*351T>C
XM_011545533.1:c.*266T>C (PHEX)	XP_011543835.1:n.*266T>C
XM_011545534.1:c.*266T>C (PHEX)	XP_011543836.1:n.*266T>C
XM_011545536.1:c.*266T>C (PHEX)	XP_011543838.1:n.*266T>C
XR_950533.1:n.140+5720A>G
XR_950534.1:n.127+5720A>G
NR_073010.2:n.850+5720A>G (PTCHD1-AS)
XM_011545536.2:c.*266T>C (PHEX)	XP_011543838.1:n.*266T>C
XM_017029579.1:c.*266T>C (PHEX)	XP_016885068.1:n.*266T>C
XM_024452390.1:c.*266T>C (PHEX)	XP_024308158.1:n.*266T>C
XR_001755695.1:n.3356T>C (PHEX)
NM_000444.6:c.*266T>C (PHEX) MANE Select	NP_000435.3:n.*266T>C
NM_001282754.2:c.*351T>C (PHEX)	NP_001269683.1:n.*351T>C