Canonical Allele Identifier: CA2419167633

Gene: PHEX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22094077G= , CM000685.2:g.22094077G=	GRCh38
NC_000023.10:g.22112195G= , CM000685.1:g.22112195G=	GRCh37
NC_000023.9:g.22022116G=	NCBI36
NG_007563.2:g.66275G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.1253G=
ENST00000684143.1:c.824G=	ENSP00000508264.1:p.Arg275=
ENST00000684745.1:n.501G=
ENST00000379374.5:c.827G= MANE Select	ENSP00000368682.4:p.Arg276=
ENST00000379374.4:c.827G=	ENSP00000368682.4:p.Arg276=
ENST00000475778.1:n.100G=
NM_000444.5:c.827G=	NP_000435.3:p.Arg276=
NM_001282754.1:c.827G=	NP_001269683.1:p.Arg276=
XM_011545533.1:c.71G=	XP_011543835.1:p.Arg24=
XM_011545534.1:c.71G=	XP_011543836.1:p.Arg24=
XM_011545535.1:c.827G=	XP_011543837.1:p.Arg276=
XM_017029579.1:c.71G=	XP_016885068.1:p.Arg24=
XM_024452390.1:c.536G=	XP_024308158.1:p.Arg179=
XR_001755695.1:n.1506G=
NM_000444.6:c.827G= MANE Select	NP_000435.3:p.Arg276=
NM_001282754.2:c.827G=	NP_001269683.1:p.Arg276=