Canonical Allele Identifier: CA412573731

Gene: PHEX PTCHD1-AS

Linked Data

• ClinVar Variation Id: 1686050
• ClinVar RCV Id: RCV002250217
• dbSNP Id: rs2147174526
• MyVariant Identifiers: chrX:g.22239801A>T (hg19) ; chrX:g.22221684A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22221684A>T , CM000685.2:g.22221684A>T	GRCh38
NC_000023.10:g.22239801A>T , CM000685.1:g.22239801A>T	GRCh37
NC_000023.9:g.22149722A>T	NCBI36
NG_007563.2:g.193881A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682888.1:c.394A>T (PHEX)	ENSP00000508003.1:p.Lys132Ter
ENST00000683162.1:c.394A>T (PHEX)	ENSP00000508059.1:p.Lys132Ter
ENST00000683289.1:c.394A>T (PHEX)	ENSP00000508195.1:p.Lys132Ter
ENST00000683917.1:n.624A>T (PHEX)
ENST00000684356.1:c.394A>T (PHEX)	ENSP00000507619.1:p.Lys132Ter
ENST00000684745.1:n.1514A>T (PHEX)
ENST00000379374.5:c.1840A>T (PHEX) MANE Select	ENSP00000368682.4:p.Lys614Ter
ENST00000379374.4:c.1840A>T (PHEX)	ENSP00000368682.4:p.Lys614Ter
NM_000444.5:c.1840A>T (PHEX)	NP_000435.3:p.Lys614Ter
NM_001282754.1:c.1840A>T (PHEX)	NP_001269683.1:p.Lys614Ter
XM_011545533.1:c.1084A>T (PHEX)	XP_011543835.1:p.Lys362Ter
XM_011545534.1:c.1084A>T (PHEX)	XP_011543836.1:p.Lys362Ter
XM_011545536.1:c.733A>T (PHEX)	XP_011543838.1:p.Lys245Ter
NR_073010.2:n.1048+5786T>A (PTCHD1-AS)
XM_011545536.2:c.733A>T (PHEX)	XP_011543838.1:p.Lys245Ter
XM_017029579.1:c.1084A>T (PHEX)	XP_016885068.1:p.Lys362Ter
XM_024452390.1:c.1549A>T (PHEX)	XP_024308158.1:p.Lys517Ter
XR_001755695.1:n.2680A>T (PHEX)
NM_000444.6:c.1840A>T (PHEX) MANE Select	NP_000435.3:p.Lys614Ter
NM_001282754.2:c.1840A>T (PHEX)	NP_001269683.1:p.Lys614Ter