Canonical Allele Identifier: CA2693304808

Gene: PHEX

Linked Data

• gnomAD v4: X-22096807-C-CTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22096810_22096814dup , CM000685.2:g.22096810_22096814dup	GRCh38
NC_000023.10:g.22114928_22114932dup , CM000685.1:g.22114928_22114932dup	GRCh37
NC_000023.9:g.22024849_22024853dup	NCBI36
NG_007563.2:g.69008_69012dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000475778.2:n.1276-145_1276-141dup
ENST00000684143.1:c.847-145_847-141dup	ENSP00000508264.1:n.847-145_847-141dup
ENST00000684745.1:n.524-145_524-141dup
ENST00000379374.5:c.850-145_850-141dup MANE Select	ENSP00000368682.4:n.850-145_850-141dup
ENST00000379374.4:c.850-145_850-141dup	ENSP00000368682.4:n.850-145_850-141dup
ENST00000475778.1:n.123-145_123-141dup
NM_000444.5:c.850-145_850-141dup	NP_000435.3:n.850-145_850-141dup
NM_001282754.1:c.850-145_850-141dup	NP_001269683.1:n.850-145_850-141dup
XM_011545533.1:c.94-145_94-141dup	XP_011543835.1:n.94-145_94-141dup
XM_011545534.1:c.94-145_94-141dup	XP_011543836.1:n.94-145_94-141dup
XM_011545535.1:c.850-145_850-141dup	XP_011543837.1:n.850-145_850-141dup
XM_017029579.1:c.94-145_94-141dup	XP_016885068.1:n.94-145_94-141dup
XM_024452390.1:c.559-145_559-141dup	XP_024308158.1:n.559-145_559-141dup
XR_001755695.1:n.1529-145_1529-141dup
NM_000444.6:c.850-145_850-141dup MANE Select	NP_000435.3:n.850-145_850-141dup
NM_001282754.2:c.850-145_850-141dup	NP_001269683.1:n.850-145_850-141dup