Canonical Allele Identifier: CA3065189090

Gene: PHEX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22099118A= , CM000685.2:g.22099118A=	GRCh38
NC_000023.10:g.22117236A= , CM000685.1:g.22117236A=	GRCh37
NC_000023.9:g.22027157A=	NCBI36
NG_007563.2:g.71316A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.1472A=
ENST00000684143.1:c.1043A=	ENSP00000508264.1:p.Asp348=
ENST00000684745.1:n.720A=
ENST00000379374.5:c.1046A= MANE Select	ENSP00000368682.4:p.Asp349=
ENST00000379374.4:c.1046A=	ENSP00000368682.4:p.Asp349=
ENST00000475778.1:n.319A=
NM_000444.5:c.1046A=	NP_000435.3:p.Asp349=
NM_001282754.1:c.1046A=	NP_001269683.1:p.Asp349=
XM_011545533.1:c.290A=	XP_011543835.1:p.Asp97=
XM_011545534.1:c.290A=	XP_011543836.1:p.Asp97=
XM_011545535.1:c.1046A=	XP_011543837.1:p.Asp349=
XM_017029579.1:c.290A=	XP_016885068.1:p.Asp97=
XM_024452390.1:c.755A=	XP_024308158.1:p.Asp252=
XR_001755695.1:n.1725A=
NM_000444.6:c.1046A= MANE Select	NP_000435.3:p.Asp349=
NM_001282754.2:c.1046A=	NP_001269683.1:p.Asp349=