Canonical Allele Identifier: CA2419162355

Gene: PHEX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22077539G= , CM000685.2:g.22077539G=	GRCh38
NC_000023.10:g.22095657G= , CM000685.1:g.22095657G=	GRCh37
NC_000023.9:g.22005578G=	NCBI36
NG_007563.2:g.49737G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.926G=
ENST00000683214.1:n.608G=
ENST00000684143.1:c.497G=	ENSP00000508264.1:p.Trp166=
ENST00000684745.1:n.174G=
ENST00000379374.5:c.500G= MANE Select	ENSP00000368682.4:p.Trp167=
ENST00000379374.4:c.500G=	ENSP00000368682.4:p.Trp167=
NM_000444.5:c.500G=	NP_000435.3:p.Trp167=
NM_001282754.1:c.500G=	NP_001269683.1:p.Trp167=
XM_011545535.1:c.500G=	XP_011543837.1:p.Trp167=
XM_017029579.1:c.-93-12890G=	XP_016885068.1:n.-93-12890G=
XM_024452390.1:c.209G=	XP_024308158.1:p.Trp70=
XR_001755695.1:n.1179G=
NM_000444.6:c.500G= MANE Select	NP_000435.3:p.Trp167=
NM_001282754.2:c.500G=	NP_001269683.1:p.Trp167=