Canonical Allele Identifier: CA2419167564

Gene: PHEX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22093867C= , CM000685.2:g.22093867C=	GRCh38
NC_000023.10:g.22111985C= , CM000685.1:g.22111985C=	GRCh37
NC_000023.9:g.22021906C=	NCBI36
NG_007563.2:g.66065C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.1159-116C=
ENST00000684143.1:c.730-116C=	ENSP00000508264.1:n.730-116C=
ENST00000684745.1:n.407-116C=
ENST00000379374.5:c.733-116C= MANE Select	ENSP00000368682.4:n.733-116C=
ENST00000379374.4:c.733-116C=	ENSP00000368682.4:n.733-116C=
ENST00000475778.1:n.6-116C=
NM_000444.5:c.733-116C=	NP_000435.3:n.733-116C=
NM_001282754.1:c.733-116C=	NP_001269683.1:n.733-116C=
XM_011545533.1:c.-24-116C=	XP_011543835.1:n.-24-116C=
XM_011545534.1:c.-24-116C=	XP_011543836.1:n.-24-116C=
XM_011545535.1:c.733-116C=	XP_011543837.1:n.733-116C=
XM_017029579.1:c.-24-116C=	XP_016885068.1:n.-24-116C=
XM_024452390.1:c.442-116C=	XP_024308158.1:n.442-116C=
XR_001755695.1:n.1412-116C=
NM_000444.6:c.733-116C= MANE Select	NP_000435.3:n.733-116C=
NM_001282754.2:c.733-116C=	NP_001269683.1:n.733-116C=