Canonical Allele Identifier: CA2419152329

Gene: PHEX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22047011A= , CM000685.2:g.22047011A=	GRCh38
NC_000023.10:g.22065129A= , CM000685.1:g.22065129A=	GRCh37
NC_000023.9:g.21975050A=	NCBI36
NG_007563.2:g.19209A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000475778.2:n.614-39A=
ENST00000683214.1:n.544+13888A=
ENST00000684143.1:c.188-39A=	ENSP00000508264.1:n.188-39A=
ENST00000379374.5:c.188-39A= MANE Select	ENSP00000368682.4:n.188-39A=
ENST00000379374.4:c.188-39A=	ENSP00000368682.4:n.188-39A=
NM_000444.5:c.188-39A=	NP_000435.3:n.188-39A=
NM_001282754.1:c.188-39A=	NP_001269683.1:n.188-39A=
XM_011545535.1:c.188-39A=	XP_011543837.1:n.188-39A=
XM_024452390.1:c.-104-39A=	XP_024308158.1:n.-104-39A=
XR_001755695.1:n.867-39A=
NM_000444.6:c.188-39A= MANE Select	NP_000435.3:n.188-39A=
NM_001282754.2:c.188-39A=	NP_001269683.1:n.188-39A=