Canonical Allele Identifier: CA2419162008

Gene: PHEX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22076494A= , CM000685.2:g.22076494A=	GRCh38
NC_000023.10:g.22094612A= , CM000685.1:g.22094612A=	GRCh37
NC_000023.9:g.22004533A=	NCBI36
NG_007563.2:g.48692A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.862+20A=
ENST00000683214.1:n.545-982A=
ENST00000684143.1:c.436+20A=	ENSP00000508264.1:n.436+20A=
ENST00000684745.1:n.113+20A=
ENST00000379374.5:c.436+20A= MANE Select	ENSP00000368682.4:n.436+20A=
ENST00000379374.4:c.436+20A=	ENSP00000368682.4:n.436+20A=
NM_000444.5:c.436+20A=	NP_000435.3:n.436+20A=
NM_001282754.1:c.436+20A=	NP_001269683.1:n.436+20A=
XM_011545535.1:c.436+20A=	XP_011543837.1:n.436+20A=
XM_017029579.1:c.-93-13935A=	XP_016885068.1:n.-93-13935A=
XM_024452390.1:c.145+20A=	XP_024308158.1:n.145+20A=
XR_001755695.1:n.1115+20A=
NM_000444.6:c.436+20A= MANE Select	NP_000435.3:n.436+20A=
NM_001282754.2:c.436+20A=	NP_001269683.1:n.436+20A=