Canonical Allele Identifier: CA2503344791

Gene: PHEX

Linked Data

• gnomAD v4: X-22178210-ATT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22178216_22178217del , CM000685.2:g.22178216_22178217del	GRCh38
NC_000023.10:g.22196333_22196334del , CM000685.1:g.22196333_22196334del	GRCh37
NC_000023.9:g.22106254_22106255del	NCBI36
NG_007563.2:g.150413_150414del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682888.1:c.37-57_37-56del	ENSP00000508003.1:n.37-57_37-56del
ENST00000683162.1:c.37-57_37-56del	ENSP00000508059.1:n.37-57_37-56del
ENST00000683289.1:c.37-57_37-56del	ENSP00000508195.1:n.37-57_37-56del
ENST00000683917.1:n.267-57_267-56del
ENST00000684356.1:c.37-57_37-56del	ENSP00000507619.1:n.37-57_37-56del
ENST00000684745.1:n.1157-57_1157-56del
ENST00000379374.5:c.1483-57_1483-56del MANE Select	ENSP00000368682.4:n.1483-57_1483-56del
ENST00000379374.4:c.1483-57_1483-56del	ENSP00000368682.4:n.1483-57_1483-56del
NM_000444.5:c.1483-57_1483-56del	NP_000435.3:n.1483-57_1483-56del
NM_001282754.1:c.1483-57_1483-56del	NP_001269683.1:n.1483-57_1483-56del
XM_011545533.1:c.727-57_727-56del	XP_011543835.1:n.727-57_727-56del
XM_011545534.1:c.727-57_727-56del	XP_011543836.1:n.727-57_727-56del
XM_011545536.1:c.376-57_376-56del	XP_011543838.1:n.376-57_376-56del
XM_011545536.2:c.376-57_376-56del	XP_011543838.1:n.376-57_376-56del
XM_017029579.1:c.727-57_727-56del	XP_016885068.1:n.727-57_727-56del
XM_024452390.1:c.1192-57_1192-56del	XP_024308158.1:n.1192-57_1192-56del
XR_001755695.1:n.2323-57_2323-56del
NM_000444.6:c.1483-57_1483-56del MANE Select	NP_000435.3:n.1483-57_1483-56del
NM_001282754.2:c.1483-57_1483-56del	NP_001269683.1:n.1483-57_1483-56del