Canonical Allele Identifier: CA10368071

Gene: PHEX

Linked Data

• dbSNP Id: rs372618065
• ExAC: X:22095790 T / C
• gnomAD v2: X-22095790-T-C
• gnomAD v4: X-22077672-T-C
• MyVariant Identifiers: chrX:g.22095790T>C (hg19) ; chrX:g.22077672T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22077672T>C , CM000685.2:g.22077672T>C	GRCh38
NC_000023.10:g.22095790T>C , CM000685.1:g.22095790T>C	GRCh37
NC_000023.9:g.22005711T>C	NCBI36
NG_007563.2:g.49870T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.1059T>C
ENST00000683214.1:n.741T>C
ENST00000684143.1:c.630T>C	ENSP00000508264.1:p.Asp210=
ENST00000684745.1:n.307T>C
ENST00000379374.5:c.633T>C MANE Select	ENSP00000368682.4:p.Asp211=
ENST00000379374.4:c.633T>C	ENSP00000368682.4:p.Asp211=
NM_000444.5:c.633T>C	NP_000435.3:p.Asp211=
NM_001282754.1:c.633T>C	NP_001269683.1:p.Asp211=
XM_011545535.1:c.633T>C	XP_011543837.1:p.Asp211=
XM_017029579.1:c.-93-12757T>C	XP_016885068.1:n.-93-12757T>C
XM_024452390.1:c.342T>C	XP_024308158.1:p.Asp114=
XR_001755695.1:n.1312T>C
NM_000444.6:c.633T>C MANE Select	NP_000435.3:p.Asp211=
NM_001282754.2:c.633T>C	NP_001269683.1:p.Asp211=