Canonical Allele Identifier: CA2693304865

Gene: PHEX

Linked Data

• gnomAD v4: X-22096923-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22096923G>A , CM000685.2:g.22096923G>A	GRCh38
NC_000023.10:g.22115041G>A , CM000685.1:g.22115041G>A	GRCh37
NC_000023.9:g.22024962G>A	NCBI36
NG_007563.2:g.69121G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000475778.2:n.1276-32G>A
ENST00000684143.1:c.847-32G>A	ENSP00000508264.1:n.847-32G>A
ENST00000684745.1:n.524-32G>A
ENST00000379374.5:c.850-32G>A MANE Select	ENSP00000368682.4:n.850-32G>A
ENST00000379374.4:c.850-32G>A	ENSP00000368682.4:n.850-32G>A
ENST00000475778.1:n.123-32G>A
NM_000444.5:c.850-32G>A	NP_000435.3:n.850-32G>A
NM_001282754.1:c.850-32G>A	NP_001269683.1:n.850-32G>A
XM_011545533.1:c.94-32G>A	XP_011543835.1:n.94-32G>A
XM_011545534.1:c.94-32G>A	XP_011543836.1:n.94-32G>A
XM_011545535.1:c.850-32G>A	XP_011543837.1:n.850-32G>A
XM_017029579.1:c.94-32G>A	XP_016885068.1:n.94-32G>A
XM_024452390.1:c.559-32G>A	XP_024308158.1:n.559-32G>A
XR_001755695.1:n.1529-32G>A
NM_000444.6:c.850-32G>A MANE Select	NP_000435.3:n.850-32G>A
NM_001282754.2:c.850-32G>A	NP_001269683.1:n.850-32G>A