Canonical Allele Identifier: CA2419152369

Gene: PHEX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22047133A= , CM000685.2:g.22047133A=	GRCh38
NC_000023.10:g.22065251A= , CM000685.1:g.22065251A=	GRCh37
NC_000023.9:g.21975172A=	NCBI36
NG_007563.2:g.19331A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.697A=
ENST00000683214.1:n.544+14010A=
ENST00000684143.1:c.271A=	ENSP00000508264.1:p.Asn91=
ENST00000379374.5:c.271A= MANE Select	ENSP00000368682.4:p.Asn91=
ENST00000379374.4:c.271A=	ENSP00000368682.4:p.Asn91=
NM_000444.5:c.271A=	NP_000435.3:p.Asn91=
NM_001282754.1:c.271A=	NP_001269683.1:p.Asn91=
XM_011545535.1:c.271A=	XP_011543837.1:p.Asn91=
XM_024452390.1:c.-21A=	XP_024308158.1:n.-21A=
XR_001755695.1:n.950A=
NM_000444.6:c.271A= MANE Select	NP_000435.3:p.Asn91=
NM_001282754.2:c.271A=	NP_001269683.1:p.Asn91=