Canonical Allele Identifier: CA2693304162

Gene: PHEX

Linked Data

• gnomAD v4: X-22046924-TTTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22046925_22046927del , CM000685.2:g.22046925_22046927del	GRCh38
NC_000023.10:g.22065043_22065045del , CM000685.1:g.22065043_22065045del	GRCh37
NC_000023.9:g.21974964_21974966del	NCBI36
NG_007563.2:g.19123_19125del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.614-125_614-123del
ENST00000683214.1:n.544+13802_544+13804del
ENST00000684143.1:c.188-125_188-123del	ENSP00000508264.1:n.188-125_188-123del
ENST00000379374.5:c.188-125_188-123del MANE Select	ENSP00000368682.4:n.188-125_188-123del
ENST00000379374.4:c.188-125_188-123del	ENSP00000368682.4:n.188-125_188-123del
NM_000444.5:c.188-125_188-123del	NP_000435.3:n.188-125_188-123del
NM_001282754.1:c.188-125_188-123del	NP_001269683.1:n.188-125_188-123del
XM_011545535.1:c.188-125_188-123del	XP_011543837.1:n.188-125_188-123del
XM_024452390.1:c.-104-125_-104-123del	XP_024308158.1:n.-104-125_-104-123del
XR_001755695.1:n.867-125_867-123del
NM_000444.6:c.188-125_188-123del MANE Select	NP_000435.3:n.188-125_188-123del
NM_001282754.2:c.188-125_188-123del	NP_001269683.1:n.188-125_188-123del