Canonical Allele Identifier: CA515431870

Gene: PHEX

Linked Data

• MyVariant Identifiers: chrX:g.22208576G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22190459G>C , CM000685.2:g.22190459G>C	GRCh38
NC_000023.10:g.22208576G>C , CM000685.1:g.22208576G>C	GRCh37
NC_000023.9:g.22118497G>C	NCBI36
NG_007563.2:g.162656G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682888.1:c.156G>C	ENSP00000508003.1:p.Pro52=
ENST00000683162.1:c.156G>C	ENSP00000508059.1:p.Pro52=
ENST00000683289.1:c.156G>C	ENSP00000508195.1:p.Pro52=
ENST00000683917.1:n.386G>C
ENST00000684356.1:c.156G>C	ENSP00000507619.1:p.Pro52=
ENST00000684745.1:n.1276G>C
ENST00000379374.5:c.1602G>C MANE Select	ENSP00000368682.4:p.Pro534=
ENST00000379374.4:c.1602G>C	ENSP00000368682.4:p.Pro534=
NM_000444.5:c.1602G>C	NP_000435.3:p.Pro534=
NM_001282754.1:c.1602G>C	NP_001269683.1:p.Pro534=
XM_011545533.1:c.846G>C	XP_011543835.1:p.Pro282=
XM_011545534.1:c.846G>C	XP_011543836.1:p.Pro282=
XM_011545536.1:c.495G>C	XP_011543838.1:p.Pro165=
XM_011545536.2:c.495G>C	XP_011543838.1:p.Pro165=
XM_017029579.1:c.846G>C	XP_016885068.1:p.Pro282=
XM_024452390.1:c.1311G>C	XP_024308158.1:p.Pro437=
XR_001755695.1:n.2442G>C
NM_000444.6:c.1602G>C MANE Select	NP_000435.3:p.Pro534=
NM_001282754.2:c.1602G>C	NP_001269683.1:p.Pro534=