Canonical Allele Identifier: CA10603559

Gene: PHEX

Linked Data

• ClinVar Variation Id: 279869
• ClinVar RCV Id: RCV000375232
• dbSNP Id: rs886041223
• gnomAD v4: X-22093982-G-A
• MyVariant Identifiers: chrX:g.22112100G>A (hg19) ; chrX:g.22093982G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22093982G>A , CM000685.2:g.22093982G>A	GRCh38
NC_000023.10:g.22112100G>A , CM000685.1:g.22112100G>A	GRCh37
NC_000023.9:g.22022021G>A	NCBI36
NG_007563.2:g.66180G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.1159-1G>A
ENST00000684143.1:c.730-1G>A	ENSP00000508264.1:n.730-1G>A
ENST00000684745.1:n.407-1G>A
ENST00000379374.5:c.733-1G>A MANE Select	ENSP00000368682.4:n.733-1G>A
ENST00000379374.4:c.733-1G>A	ENSP00000368682.4:n.733-1G>A
ENST00000475778.1:n.6-1G>A
NM_000444.5:c.733-1G>A	NP_000435.3:n.733-1G>A
NM_001282754.1:c.733-1G>A	NP_001269683.1:n.733-1G>A
XM_011545533.1:c.-24-1G>A	XP_011543835.1:n.-24-1G>A
XM_011545534.1:c.-24-1G>A	XP_011543836.1:n.-24-1G>A
XM_011545535.1:c.733-1G>A	XP_011543837.1:n.733-1G>A
XM_017029579.1:c.-24-1G>A	XP_016885068.1:n.-24-1G>A
XM_024452390.1:c.442-1G>A	XP_024308158.1:n.442-1G>A
XR_001755695.1:n.1412-1G>A
NM_000444.6:c.733-1G>A MANE Select	NP_000435.3:n.733-1G>A
NM_001282754.2:c.733-1G>A	NP_001269683.1:n.733-1G>A