Canonical Allele Identifier: CA2419161953

Gene: PHEX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22077653G= , CM000685.2:g.22077653G=	GRCh38
NC_000023.10:g.22095771G= , CM000685.1:g.22095771G=	GRCh37
NC_000023.9:g.22005692G=	NCBI36
NG_007563.2:g.49851G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000475778.2:n.1040G=
ENST00000683214.1:n.722G=
ENST00000684143.1:c.611G=	ENSP00000508264.1:p.Arg204=
ENST00000684745.1:n.288G=
ENST00000379374.5:c.614G= MANE Select	ENSP00000368682.4:p.Arg205=
ENST00000379374.4:c.614G=	ENSP00000368682.4:p.Arg205=
NM_000444.5:c.614G=	NP_000435.3:p.Arg205=
NM_001282754.1:c.614G=	NP_001269683.1:p.Arg205=
XM_011545535.1:c.614G=	XP_011543837.1:p.Arg205=
XM_017029579.1:c.-93-12776G=	XP_016885068.1:n.-93-12776G=
XM_024452390.1:c.323G=	XP_024308158.1:p.Arg108=
XR_001755695.1:n.1293G=
NM_000444.6:c.614G= MANE Select	NP_000435.3:p.Arg205=
NM_001282754.2:c.614G=	NP_001269683.1:p.Arg205=