Canonical Allele Identifier: CA515423668

Gene: PHEX

Linked Data

• dbSNP Id: rs1411877524
• gnomAD v2: X-22112133-T-C
• gnomAD v4: X-22094015-T-C
• COSMIC: COSM3406233
• MyVariant Identifiers: chrX:g.22112133T>C (hg19) ; chrX:g.22094015T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22094015T>C , CM000685.2:g.22094015T>C	GRCh38
NC_000023.10:g.22112133T>C , CM000685.1:g.22112133T>C	GRCh37
NC_000023.9:g.22022054T>C	NCBI36
NG_007563.2:g.66213T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000475778.2:n.1191T>C
ENST00000684143.1:c.762T>C	ENSP00000508264.1:p.Asp254=
ENST00000684745.1:n.439T>C
ENST00000379374.5:c.765T>C MANE Select	ENSP00000368682.4:p.Asp255=
ENST00000379374.4:c.765T>C	ENSP00000368682.4:p.Asp255=
ENST00000475778.1:n.38T>C
NM_000444.5:c.765T>C	NP_000435.3:p.Asp255=
NM_001282754.1:c.765T>C	NP_001269683.1:p.Asp255=
XM_011545533.1:c.9T>C	XP_011543835.1:p.Asp3=
XM_011545534.1:c.9T>C	XP_011543836.1:p.Asp3=
XM_011545535.1:c.765T>C	XP_011543837.1:p.Asp255=
XM_017029579.1:c.9T>C	XP_016885068.1:p.Asp3=
XM_024452390.1:c.474T>C	XP_024308158.1:p.Asp158=
XR_001755695.1:n.1444T>C
NM_000444.6:c.765T>C MANE Select	NP_000435.3:p.Asp255=
NM_001282754.2:c.765T>C	NP_001269683.1:p.Asp255=