Canonical Allele Identifier: CA2693304359

Gene: PHEX

Linked Data

• gnomAD v4: X-22076535-ATGTTTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22076536_22076541del , CM000685.2:g.22076536_22076541del	GRCh38
NC_000023.10:g.22094654_22094659del , CM000685.1:g.22094654_22094659del	GRCh37
NC_000023.9:g.22004575_22004580del	NCBI36
NG_007563.2:g.48734_48739del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.862+62_862+67del
ENST00000683214.1:n.545-940_545-935del
ENST00000684143.1:c.436+62_436+67del	ENSP00000508264.1:n.436+62_436+67del
ENST00000684745.1:n.113+62_113+67del
ENST00000379374.5:c.436+62_436+67del MANE Select	ENSP00000368682.4:n.436+62_436+67del
ENST00000379374.4:c.436+62_436+67del	ENSP00000368682.4:n.436+62_436+67del
NM_000444.5:c.436+62_436+67del	NP_000435.3:n.436+62_436+67del
NM_001282754.1:c.436+62_436+67del	NP_001269683.1:n.436+62_436+67del
XM_011545535.1:c.436+62_436+67del	XP_011543837.1:n.436+62_436+67del
XM_017029579.1:c.-93-13893_-93-13888del	XP_016885068.1:n.-93-13893_-93-13888del
XM_024452390.1:c.145+62_145+67del	XP_024308158.1:n.145+62_145+67del
XR_001755695.1:n.1115+62_1115+67del
NM_000444.6:c.436+62_436+67del MANE Select	NP_000435.3:n.436+62_436+67del
NM_001282754.2:c.436+62_436+67del	NP_001269683.1:n.436+62_436+67del