Canonical Allele Identifier: CA412572456

Gene: PHEX

Linked Data

• gnomAD v4: X-22094073-C-A
• MyVariant Identifiers: chrX:g.22112191C>A (hg19) ; chrX:g.22094073C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22094073C>A , CM000685.2:g.22094073C>A	GRCh38
NC_000023.10:g.22112191C>A , CM000685.1:g.22112191C>A	GRCh37
NC_000023.9:g.22022112C>A	NCBI36
NG_007563.2:g.66271C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.1249C>A
ENST00000684143.1:c.820C>A	ENSP00000508264.1:p.Leu274Ile
ENST00000684745.1:n.497C>A
ENST00000379374.5:c.823C>A MANE Select	ENSP00000368682.4:p.Leu275Ile
ENST00000379374.4:c.823C>A	ENSP00000368682.4:p.Leu275Ile
ENST00000475778.1:n.96C>A
NM_000444.5:c.823C>A	NP_000435.3:p.Leu275Ile
NM_001282754.1:c.823C>A	NP_001269683.1:p.Leu275Ile
XM_011545533.1:c.67C>A	XP_011543835.1:p.Leu23Ile
XM_011545534.1:c.67C>A	XP_011543836.1:p.Leu23Ile
XM_011545535.1:c.823C>A	XP_011543837.1:p.Leu275Ile
XM_017029579.1:c.67C>A	XP_016885068.1:p.Leu23Ile
XM_024452390.1:c.532C>A	XP_024308158.1:p.Leu178Ile
XR_001755695.1:n.1502C>A
NM_000444.6:c.823C>A MANE Select	NP_000435.3:p.Leu275Ile
NM_001282754.2:c.823C>A	NP_001269683.1:p.Leu275Ile