Canonical Allele Identifier: CA327520766

Gene: PHEX

Linked Data

• dbSNP Id: rs922849110
• gnomAD v3: X-22076340-G-A
• gnomAD v4: X-22076340-G-A
• MyVariant Identifiers: chrX:g.22094458G>A (hg19) ; chrX:g.22076340G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22076340G>A , CM000685.2:g.22076340G>A	GRCh38
NC_000023.10:g.22094458G>A , CM000685.1:g.22094458G>A	GRCh37
NC_000023.9:g.22004379G>A	NCBI36
NG_007563.2:g.48538G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.776-48G>A
ENST00000683214.1:n.545-1136G>A
ENST00000684143.1:c.350-48G>A	ENSP00000508264.1:n.350-48G>A
ENST00000684745.1:n.27-48G>A
ENST00000379374.5:c.350-48G>A MANE Select	ENSP00000368682.4:n.350-48G>A
ENST00000379374.4:c.350-48G>A	ENSP00000368682.4:n.350-48G>A
NM_000444.5:c.350-48G>A	NP_000435.3:n.350-48G>A
NM_001282754.1:c.350-48G>A	NP_001269683.1:n.350-48G>A
XM_011545535.1:c.350-48G>A	XP_011543837.1:n.350-48G>A
XM_017029579.1:c.-93-14089G>A	XP_016885068.1:n.-93-14089G>A
XM_024452390.1:c.59-48G>A	XP_024308158.1:n.59-48G>A
XR_001755695.1:n.1029-48G>A
NM_000444.6:c.350-48G>A MANE Select	NP_000435.3:n.350-48G>A
NM_001282754.2:c.350-48G>A	NP_001269683.1:n.350-48G>A