Canonical Allele Identifier: CA412575529

Gene: PHEX PTCHD1-AS

Linked Data

• gnomAD v4: X-22247931-T-C
• MyVariant Identifiers: chrX:g.22266048T>C (hg19) ; chrX:g.22247931T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22247931T>C , CM000685.2:g.22247931T>C	GRCh38
NC_000023.10:g.22266048T>C , CM000685.1:g.22266048T>C	GRCh37
NC_000023.9:g.22175969T>C	NCBI36
NG_007563.2:g.220128T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683162.1:c.*166T>C (PHEX)	ENSP00000508059.1:n.*166T>C
ENST00000683289.1:c.624+20320T>C (PHEX)	ENSP00000508195.1:n.624+20320T>C
ENST00000683917.1:n.1012T>C (PHEX)
ENST00000684356.1:c.782T>C (PHEX)	ENSP00000507619.1:p.Met261Thr
ENST00000684745.1:n.1902T>C (PHEX)
ENST00000379374.5:c.2228T>C (PHEX) MANE Select	ENSP00000368682.4:p.Met743Thr
ENST00000379374.4:c.2228T>C (PHEX)	ENSP00000368682.4:p.Met743Thr
NM_000444.5:c.2228T>C (PHEX)	NP_000435.3:p.Met743Thr
NM_001282754.1:c.*63T>C (PHEX)	NP_001269683.1:n.*63T>C
XM_011545533.1:c.1472T>C (PHEX)	XP_011543835.1:p.Met491Thr
XM_011545534.1:c.1472T>C (PHEX)	XP_011543836.1:p.Met491Thr
XM_011545536.1:c.1121T>C (PHEX)	XP_011543838.1:p.Met374Thr
XR_950533.1:n.140+6008A>G
XR_950534.1:n.127+6008A>G
NR_073010.2:n.850+6008A>G (PTCHD1-AS)
XM_011545536.2:c.1121T>C (PHEX)	XP_011543838.1:p.Met374Thr
XM_017029579.1:c.1472T>C (PHEX)	XP_016885068.1:p.Met491Thr
XM_024452390.1:c.1937T>C (PHEX)	XP_024308158.1:p.Met646Thr
XR_001755695.1:n.3068T>C (PHEX)
NM_000444.6:c.2228T>C (PHEX) MANE Select	NP_000435.3:p.Met743Thr
NM_001282754.2:c.*63T>C (PHEX)	NP_001269683.1:n.*63T>C