Canonical Allele Identifier: CA2693308512

Gene: PHEX PTCHD1-AS

Linked Data

• gnomAD v4: X-22248022-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22248022T>G , CM000685.2:g.22248022T>G	GRCh38
NC_000023.10:g.22266139T>G , CM000685.1:g.22266139T>G	GRCh37
NC_000023.9:g.22176060T>G	NCBI36
NG_007563.2:g.220219T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683162.1:c.*257T>G (PHEX)	ENSP00000508059.1:n.*257T>G
ENST00000683289.1:c.624+20411T>G (PHEX)	ENSP00000508195.1:n.624+20411T>G
ENST00000683917.1:n.1103T>G (PHEX)
ENST00000684356.1:c.*69T>G (PHEX)	ENSP00000507619.1:n.*69T>G
ENST00000684745.1:n.1993T>G (PHEX)
ENST00000379374.5:c.*69T>G (PHEX) MANE Select	ENSP00000368682.4:n.*69T>G
ENST00000379374.4:c.*69T>G (PHEX)	ENSP00000368682.4:n.*69T>G
NM_000444.5:c.*69T>G (PHEX)	NP_000435.3:n.*69T>G
NM_001282754.1:c.*154T>G (PHEX)	NP_001269683.1:n.*154T>G
XM_011545533.1:c.*69T>G (PHEX)	XP_011543835.1:n.*69T>G
XM_011545534.1:c.*69T>G (PHEX)	XP_011543836.1:n.*69T>G
XM_011545536.1:c.*69T>G (PHEX)	XP_011543838.1:n.*69T>G
XR_950533.1:n.140+5917A>C
XR_950534.1:n.127+5917A>C
NR_073010.2:n.850+5917A>C (PTCHD1-AS)
XM_011545536.2:c.*69T>G (PHEX)	XP_011543838.1:n.*69T>G
XM_017029579.1:c.*69T>G (PHEX)	XP_016885068.1:n.*69T>G
XM_024452390.1:c.*69T>G (PHEX)	XP_024308158.1:n.*69T>G
XR_001755695.1:n.3159T>G (PHEX)
NM_000444.6:c.*69T>G (PHEX) MANE Select	NP_000435.3:n.*69T>G
NM_001282754.2:c.*154T>G (PHEX)	NP_001269683.1:n.*154T>G