Canonical Allele Identifier: CA2419168601

Gene: PHEX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22097007A= , CM000685.2:g.22097007A=	GRCh38
NC_000023.10:g.22115125A= , CM000685.1:g.22115125A=	GRCh37
NC_000023.9:g.22025046A=	NCBI36
NG_007563.2:g.69205A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000475778.2:n.1328A=
ENST00000684143.1:c.899A=	ENSP00000508264.1:p.Asn300=
ENST00000684745.1:n.576A=
ENST00000379374.5:c.902A= MANE Select	ENSP00000368682.4:p.Asn301=
ENST00000379374.4:c.902A=	ENSP00000368682.4:p.Asn301=
ENST00000475778.1:n.175A=
NM_000444.5:c.902A=	NP_000435.3:p.Asn301=
NM_001282754.1:c.902A=	NP_001269683.1:p.Asn301=
XM_011545533.1:c.146A=	XP_011543835.1:p.Asn49=
XM_011545534.1:c.146A=	XP_011543836.1:p.Asn49=
XM_011545535.1:c.902A=	XP_011543837.1:p.Asn301=
XM_017029579.1:c.146A=	XP_016885068.1:p.Asn49=
XM_024452390.1:c.611A=	XP_024308158.1:p.Asn204=
XR_001755695.1:n.1581A=
NM_000444.6:c.902A= MANE Select	NP_000435.3:p.Asn301=
NM_001282754.2:c.902A=	NP_001269683.1:p.Asn301=