Canonical Allele Identifier: CA412567537

Gene: PHEX

Linked Data

• MyVariant Identifiers: chrX:g.22065191A>C (hg19) ; chrX:g.22047073A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22047073A>C , CM000685.2:g.22047073A>C	GRCh38
NC_000023.10:g.22065191A>C , CM000685.1:g.22065191A>C	GRCh37
NC_000023.9:g.21975112A>C	NCBI36
NG_007563.2:g.19271A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.637A>C
ENST00000683214.1:n.544+13950A>C
ENST00000684143.1:c.211A>C	ENSP00000508264.1:p.Asn71His
ENST00000379374.5:c.211A>C MANE Select	ENSP00000368682.4:p.Asn71His
ENST00000379374.4:c.211A>C	ENSP00000368682.4:p.Asn71His
NM_000444.5:c.211A>C	NP_000435.3:p.Asn71His
NM_001282754.1:c.211A>C	NP_001269683.1:p.Asn71His
XM_011545535.1:c.211A>C	XP_011543837.1:p.Asn71His
XM_024452390.1:c.-81A>C	XP_024308158.1:n.-81A>C
XR_001755695.1:n.890A>C
NM_000444.6:c.211A>C MANE Select	NP_000435.3:p.Asn71His
NM_001282754.2:c.211A>C	NP_001269683.1:p.Asn71His