Canonical Allele Identifier: CA412574576

Gene: PHEX

Linked Data

• ClinVar Variation Id: 1525455
• ClinVar RCV Id: RCV002036699
• dbSNP Id: rs777167473
• MyVariant Identifiers: chrX:g.22151661G>T (hg19) ; chrX:g.22133544G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22133544G>T , CM000685.2:g.22133544G>T	GRCh38
NC_000023.10:g.22151661G>T , CM000685.1:g.22151661G>T	GRCh37
NC_000023.9:g.22061582G>T	NCBI36
NG_007563.2:g.105741G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000684745.1:n.998G>T
ENST00000379374.5:c.1324G>T MANE Select	ENSP00000368682.4:p.Val442Phe
ENST00000379374.4:c.1324G>T	ENSP00000368682.4:p.Val442Phe
NM_000444.5:c.1324G>T	NP_000435.3:p.Val442Phe
NM_001282754.1:c.1324G>T	NP_001269683.1:p.Val442Phe
XM_011545533.1:c.568G>T	XP_011543835.1:p.Val190Phe
XM_011545534.1:c.568G>T	XP_011543836.1:p.Val190Phe
XM_011545535.1:c.1324G>T	XP_011543837.1:p.Val442Phe
XM_011545536.1:c.217G>T	XP_011543838.1:p.Val73Phe
XM_011545536.2:c.217G>T	XP_011543838.1:p.Val73Phe
XM_017029579.1:c.568G>T	XP_016885068.1:p.Val190Phe
XM_024452390.1:c.1033G>T	XP_024308158.1:p.Val345Phe
XR_001755695.1:n.2003G>T
NM_000444.6:c.1324G>T MANE Select	NP_000435.3:p.Val442Phe
NM_001282754.2:c.1324G>T	NP_001269683.1:p.Val442Phe