Canonical Allele Identifier: CA2419162006

Gene: PHEX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22077703G= , CM000685.2:g.22077703G=	GRCh38
NC_000023.10:g.22095821G= , CM000685.1:g.22095821G=	GRCh37
NC_000023.9:g.22005742G=	NCBI36
NG_007563.2:g.49901G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.1089+1G=
ENST00000683214.1:n.772G=
ENST00000684143.1:c.660+1G=	ENSP00000508264.1:n.660+1G=
ENST00000684745.1:n.337+1G=
ENST00000379374.5:c.663+1G= MANE Select	ENSP00000368682.4:n.663+1G=
ENST00000379374.4:c.663+1G=	ENSP00000368682.4:n.663+1G=
NM_000444.5:c.663+1G=	NP_000435.3:n.663+1G=
NM_001282754.1:c.663+1G=	NP_001269683.1:n.663+1G=
XM_011545535.1:c.663+1G=	XP_011543837.1:n.663+1G=
XM_017029579.1:c.-93-12726G=	XP_016885068.1:n.-93-12726G=
XM_024452390.1:c.372+1G=	XP_024308158.1:n.372+1G=
XR_001755695.1:n.1342+1G=
NM_000444.6:c.663+1G= MANE Select	NP_000435.3:n.663+1G=
NM_001282754.2:c.663+1G=	NP_001269683.1:n.663+1G=