Canonical Allele Identifier: CA412575484

Gene: PHEX PTCHD1-AS

Linked Data

• MyVariant Identifiers: chrX:g.22266029T>A (hg19) ; chrX:g.22247912T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22247912T>A , CM000685.2:g.22247912T>A	GRCh38
NC_000023.10:g.22266029T>A , CM000685.1:g.22266029T>A	GRCh37
NC_000023.9:g.22175950T>A	NCBI36
NG_007563.2:g.220109T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683162.1:c.*147T>A (PHEX)	ENSP00000508059.1:n.*147T>A
ENST00000683289.1:c.624+20301T>A (PHEX)	ENSP00000508195.1:n.624+20301T>A
ENST00000683917.1:n.993T>A (PHEX)
ENST00000684356.1:c.763T>A (PHEX)	ENSP00000507619.1:p.Ser255Thr
ENST00000684745.1:n.1883T>A (PHEX)
ENST00000379374.5:c.2209T>A (PHEX) MANE Select	ENSP00000368682.4:p.Ser737Thr
ENST00000379374.4:c.2209T>A (PHEX)	ENSP00000368682.4:p.Ser737Thr
NM_000444.5:c.2209T>A (PHEX)	NP_000435.3:p.Ser737Thr
NM_001282754.1:c.*44T>A (PHEX)	NP_001269683.1:n.*44T>A
XM_011545533.1:c.1453T>A (PHEX)	XP_011543835.1:p.Ser485Thr
XM_011545534.1:c.1453T>A (PHEX)	XP_011543836.1:p.Ser485Thr
XM_011545536.1:c.1102T>A (PHEX)	XP_011543838.1:p.Ser368Thr
XR_950533.1:n.140+6027A>T
XR_950534.1:n.127+6027A>T
NR_073010.2:n.850+6027A>T (PTCHD1-AS)
XM_011545536.2:c.1102T>A (PHEX)	XP_011543838.1:p.Ser368Thr
XM_017029579.1:c.1453T>A (PHEX)	XP_016885068.1:p.Ser485Thr
XM_024452390.1:c.1918T>A (PHEX)	XP_024308158.1:p.Ser640Thr
XR_001755695.1:n.3049T>A (PHEX)
NM_000444.6:c.2209T>A (PHEX) MANE Select	NP_000435.3:p.Ser737Thr
NM_001282754.2:c.*44T>A (PHEX)	NP_001269683.1:n.*44T>A