Canonical Allele Identifier: CA2419195579

Gene: PHEX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22178312C= , CM000685.2:g.22178312C=	GRCh38
NC_000023.10:g.22196429C= , CM000685.1:g.22196429C=	GRCh37
NC_000023.9:g.22106350C=	NCBI36
NG_007563.2:g.150509C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682888.1:c.76C=	ENSP00000508003.1:p.Gln26=
ENST00000683162.1:c.76C=	ENSP00000508059.1:p.Gln26=
ENST00000683289.1:c.76C=	ENSP00000508195.1:p.Gln26=
ENST00000683917.1:n.306C=
ENST00000684356.1:c.76C=	ENSP00000507619.1:p.Gln26=
ENST00000684745.1:n.1196C=
ENST00000379374.5:c.1522C= MANE Select	ENSP00000368682.4:p.Gln508=
ENST00000379374.4:c.1522C=	ENSP00000368682.4:p.Gln508=
NM_000444.5:c.1522C=	NP_000435.3:p.Gln508=
NM_001282754.1:c.1522C=	NP_001269683.1:p.Gln508=
XM_011545533.1:c.766C=	XP_011543835.1:p.Gln256=
XM_011545534.1:c.766C=	XP_011543836.1:p.Gln256=
XM_011545536.1:c.415C=	XP_011543838.1:p.Gln139=
XM_011545536.2:c.415C=	XP_011543838.1:p.Gln139=
XM_017029579.1:c.766C=	XP_016885068.1:p.Gln256=
XM_024452390.1:c.1231C=	XP_024308158.1:p.Gln411=
XR_001755695.1:n.2362C=
NM_000444.6:c.1522C= MANE Select	NP_000435.3:p.Gln508=
NM_001282754.2:c.1522C=	NP_001269683.1:p.Gln508=