Canonical Allele Identifier: CA515427430

Gene: PHEX PTCHD1-AS

Linked Data

• MyVariant Identifiers: chrX:g.22245626T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22227509T>G , CM000685.2:g.22227509T>G	GRCh38
NC_000023.10:g.22245626T>G , CM000685.1:g.22245626T>G	GRCh37
NC_000023.9:g.22155547T>G	NCBI36
NG_007563.2:g.199706T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000683162.1:c.522T>G (PHEX)	ENSP00000508059.1:p.Ala174=
ENST00000683289.1:c.522T>G (PHEX)	ENSP00000508195.1:p.Ala174=
ENST00000683917.1:n.752T>G (PHEX)
ENST00000684356.1:c.522T>G (PHEX)	ENSP00000507619.1:p.Ala174=
ENST00000684745.1:n.1642T>G (PHEX)
ENST00000379374.5:c.1968T>G (PHEX) MANE Select	ENSP00000368682.4:p.Ala656=
ENST00000379374.4:c.1968T>G (PHEX)	ENSP00000368682.4:p.Ala656=
NM_000444.5:c.1968T>G (PHEX)	NP_000435.3:p.Ala656=
NM_001282754.1:c.1968T>G (PHEX)	NP_001269683.1:p.Ala656=
XM_011545533.1:c.1212T>G (PHEX)	XP_011543835.1:p.Ala404=
XM_011545534.1:c.1212T>G (PHEX)	XP_011543836.1:p.Ala404=
XM_011545536.1:c.861T>G (PHEX)	XP_011543838.1:p.Ala287=
XR_950534.1:n.286A>C
NR_073010.2:n.1009A>C (PTCHD1-AS)
XM_011545536.2:c.861T>G (PHEX)	XP_011543838.1:p.Ala287=
XM_017029579.1:c.1212T>G (PHEX)	XP_016885068.1:p.Ala404=
XM_024452390.1:c.1677T>G (PHEX)	XP_024308158.1:p.Ala559=
XR_001755695.1:n.2808T>G (PHEX)
NM_000444.6:c.1968T>G (PHEX) MANE Select	NP_000435.3:p.Ala656=
NM_001282754.2:c.1968T>G (PHEX)	NP_001269683.1:p.Ala656=