Canonical Allele Identifier: CA515425058
Gene: PHEX HGNC NCBI

Linked Data

gnomAD v4: X-22047198-C-T
MyVariant Identifiers: chrX:g.22065316C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22047198C>T , CM000685.2:g.22047198C>T GRCh38
NC_000023.10:g.22065316C>T , CM000685.1:g.22065316C>T GRCh37
NC_000023.9:g.21975237C>T NCBI36
NG_007563.2:g.19396C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000475778.2:n.762C>T
ENST00000683214.1:n.544+14075C>T
ENST00000684143.1:c.336C>T ENSP00000508264.1:p.Asp112=
ENST00000379374.5:c.336C>T MANE Select ENSP00000368682.4:p.Asp112=
ENST00000379374.4:c.336C>T ENSP00000368682.4:p.Asp112=
NM_000444.5:c.336C>T NP_000435.3:p.Asp112=
NM_001282754.1:c.336C>T NP_001269683.1:p.Asp112=
XM_011545535.1:c.336C>T XP_011543837.1:p.Asp112=
XM_017029579.1:c.-107C>T XP_016885068.1:n.-107C>T
XM_024452390.1:c.45C>T XP_024308158.1:p.Asp15=
XR_001755695.1:n.1015C>T
NM_000444.6:c.336C>T MANE Select NP_000435.3:p.Asp112=
NM_001282754.2:c.336C>T NP_001269683.1:p.Asp112=