Canonical Allele Identifier: CA2419168590

Gene: PHEX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22096984C= , CM000685.2:g.22096984C=	GRCh38
NC_000023.10:g.22115102C= , CM000685.1:g.22115102C=	GRCh37
NC_000023.9:g.22025023C=	NCBI36
NG_007563.2:g.69182C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.1305C=
ENST00000684143.1:c.876C=	ENSP00000508264.1:p.Ser292=
ENST00000684745.1:n.553C=
ENST00000379374.5:c.879C= MANE Select	ENSP00000368682.4:p.Ser293=
ENST00000379374.4:c.879C=	ENSP00000368682.4:p.Ser293=
ENST00000475778.1:n.152C=
NM_000444.5:c.879C=	NP_000435.3:p.Ser293=
NM_001282754.1:c.879C=	NP_001269683.1:p.Ser293=
XM_011545533.1:c.123C=	XP_011543835.1:p.Ser41=
XM_011545534.1:c.123C=	XP_011543836.1:p.Ser41=
XM_011545535.1:c.879C=	XP_011543837.1:p.Ser293=
XM_017029579.1:c.123C=	XP_016885068.1:p.Ser41=
XM_024452390.1:c.588C=	XP_024308158.1:p.Ser196=
XR_001755695.1:n.1558C=
NM_000444.6:c.879C= MANE Select	NP_000435.3:p.Ser293=
NM_001282754.2:c.879C=	NP_001269683.1:p.Ser293=