Canonical Allele Identifier: CA2419162007

Gene: PHEX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22076493T= , CM000685.2:g.22076493T=	GRCh38
NC_000023.10:g.22094611T= , CM000685.1:g.22094611T=	GRCh37
NC_000023.9:g.22004532T=	NCBI36
NG_007563.2:g.48691T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.862+19T=
ENST00000683214.1:n.545-983T=
ENST00000684143.1:c.436+19T=	ENSP00000508264.1:n.436+19T=
ENST00000684745.1:n.113+19T=
ENST00000379374.5:c.436+19T= MANE Select	ENSP00000368682.4:n.436+19T=
ENST00000379374.4:c.436+19T=	ENSP00000368682.4:n.436+19T=
NM_000444.5:c.436+19T=	NP_000435.3:n.436+19T=
NM_001282754.1:c.436+19T=	NP_001269683.1:n.436+19T=
XM_011545535.1:c.436+19T=	XP_011543837.1:n.436+19T=
XM_017029579.1:c.-93-13936T=	XP_016885068.1:n.-93-13936T=
XM_024452390.1:c.145+19T=	XP_024308158.1:n.145+19T=
XR_001755695.1:n.1115+19T=
NM_000444.6:c.436+19T= MANE Select	NP_000435.3:n.436+19T=
NM_001282754.2:c.436+19T=	NP_001269683.1:n.436+19T=