Canonical Allele Identifier: CA412571675

Gene: PHEX

Linked Data

• MyVariant Identifiers: chrX:g.22095804A>C (hg19) ; chrX:g.22077686A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22077686A>C , CM000685.2:g.22077686A>C	GRCh38
NC_000023.10:g.22095804A>C , CM000685.1:g.22095804A>C	GRCh37
NC_000023.9:g.22005725A>C	NCBI36
NG_007563.2:g.49884A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.1073A>C
ENST00000683214.1:n.755A>C
ENST00000684143.1:c.644A>C	ENSP00000508264.1:p.Asn215Thr
ENST00000684745.1:n.321A>C
ENST00000379374.5:c.647A>C MANE Select	ENSP00000368682.4:p.Asn216Thr
ENST00000379374.4:c.647A>C	ENSP00000368682.4:p.Asn216Thr
NM_000444.5:c.647A>C	NP_000435.3:p.Asn216Thr
NM_001282754.1:c.647A>C	NP_001269683.1:p.Asn216Thr
XM_011545535.1:c.647A>C	XP_011543837.1:p.Asn216Thr
XM_017029579.1:c.-93-12743A>C	XP_016885068.1:n.-93-12743A>C
XM_024452390.1:c.356A>C	XP_024308158.1:p.Asn119Thr
XR_001755695.1:n.1326A>C
NM_000444.6:c.647A>C MANE Select	NP_000435.3:p.Asn216Thr
NM_001282754.2:c.647A>C	NP_001269683.1:p.Asn216Thr