Canonical Allele Identifier: CA412574722

Gene: PHEX

Linked Data

• ClinVar Variation Id: 860072
• ClinVar RCV Id: RCV001066316
• dbSNP Id: rs374873766
• MyVariant Identifiers: chrX:g.22151719C>G (hg19) ; chrX:g.22133602C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22133602C>G , CM000685.2:g.22133602C>G	GRCh38
NC_000023.10:g.22151719C>G , CM000685.1:g.22151719C>G	GRCh37
NC_000023.9:g.22061640C>G	NCBI36
NG_007563.2:g.105799C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684745.1:n.1056C>G
ENST00000379374.5:c.1382C>G MANE Select	ENSP00000368682.4:p.Thr461Arg
ENST00000379374.4:c.1382C>G	ENSP00000368682.4:p.Thr461Arg
NM_000444.5:c.1382C>G	NP_000435.3:p.Thr461Arg
NM_001282754.1:c.1382C>G	NP_001269683.1:p.Thr461Arg
XM_011545533.1:c.626C>G	XP_011543835.1:p.Thr209Arg
XM_011545534.1:c.626C>G	XP_011543836.1:p.Thr209Arg
XM_011545535.1:c.1382C>G	XP_011543837.1:p.Thr461Arg
XM_011545536.1:c.275C>G	XP_011543838.1:p.Thr92Arg
XM_011545536.2:c.275C>G	XP_011543838.1:p.Thr92Arg
XM_017029579.1:c.626C>G	XP_016885068.1:p.Thr209Arg
XM_024452390.1:c.1091C>G	XP_024308158.1:p.Thr364Arg
XR_001755695.1:n.2061C>G
NM_000444.6:c.1382C>G MANE Select	NP_000435.3:p.Thr461Arg
NM_001282754.2:c.1382C>G	NP_001269683.1:p.Thr461Arg