Canonical Allele Identifier: CA412567522

Gene: PHEX

Linked Data

• MyVariant Identifiers: chrX:g.22065183G>T (hg19) ; chrX:g.22047065G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22047065G>T , CM000685.2:g.22047065G>T	GRCh38
NC_000023.10:g.22065183G>T , CM000685.1:g.22065183G>T	GRCh37
NC_000023.9:g.21975104G>T	NCBI36
NG_007563.2:g.19263G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.629G>T
ENST00000683214.1:n.544+13942G>T
ENST00000684143.1:c.203G>T	ENSP00000508264.1:p.Ser68Ile
ENST00000379374.5:c.203G>T MANE Select	ENSP00000368682.4:p.Ser68Ile
ENST00000379374.4:c.203G>T	ENSP00000368682.4:p.Ser68Ile
NM_000444.5:c.203G>T	NP_000435.3:p.Ser68Ile
NM_001282754.1:c.203G>T	NP_001269683.1:p.Ser68Ile
XM_011545535.1:c.203G>T	XP_011543837.1:p.Ser68Ile
XM_024452390.1:c.-89G>T	XP_024308158.1:n.-89G>T
XR_001755695.1:n.882G>T
NM_000444.6:c.203G>T MANE Select	NP_000435.3:p.Ser68Ile
NM_001282754.2:c.203G>T	NP_001269683.1:p.Ser68Ile