Canonical Allele Identifier: CA515423859

Gene: PHEX

Linked Data

• MyVariant Identifiers: chrX:g.22051198G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22033080G>T , CM000685.2:g.22033080G>T	GRCh38
NC_000023.10:g.22051198G>T , CM000685.1:g.22051198G>T	GRCh37
NC_000023.9:g.21961119G>T	NCBI36
NG_007563.2:g.5278G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000475778.2:n.501G>T
ENST00000683214.1:n.501G>T
ENST00000684143.1:c.75G>T	ENSP00000508264.1:p.Val25=
ENST00000379374.5:c.75G>T MANE Select	ENSP00000368682.4:p.Val25=
ENST00000379374.4:c.75G>T	ENSP00000368682.4:p.Val25=
NM_000444.5:c.75G>T	NP_000435.3:p.Val25=
NM_001282754.1:c.75G>T	NP_001269683.1:p.Val25=
XM_011545535.1:c.75G>T	XP_011543837.1:p.Val25=
XR_001755695.1:n.754G>T
NM_000444.6:c.75G>T MANE Select	NP_000435.3:p.Val25=
NM_001282754.2:c.75G>T	NP_001269683.1:p.Val25=