Canonical Allele Identifier: CA2419173781

Gene: PHEX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22111561G= , CM000685.2:g.22111561G=	GRCh38
NC_000023.10:g.22129679G= , CM000685.1:g.22129679G=	GRCh37
NC_000023.9:g.22039600G=	NCBI36
NG_007563.2:g.83759G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684143.1:c.1170+1G=	ENSP00000508264.1:n.1170+1G=
ENST00000684745.1:n.847+1G=
ENST00000379374.5:c.1173+1G= MANE Select	ENSP00000368682.4:n.1173+1G=
ENST00000379374.4:c.1173+1G=	ENSP00000368682.4:n.1173+1G=
NM_000444.5:c.1173+1G=	NP_000435.3:n.1173+1G=
NM_001282754.1:c.1173+1G=	NP_001269683.1:n.1173+1G=
XM_011545533.1:c.417+1G=	XP_011543835.1:n.417+1G=
XM_011545534.1:c.417+1G=	XP_011543836.1:n.417+1G=
XM_011545535.1:c.1173+1G=	XP_011543837.1:n.1173+1G=
XM_011545536.1:c.66+1G=	XP_011543838.1:n.66+1G=
XM_011545536.2:c.66+1G=	XP_011543838.1:n.66+1G=
XM_017029579.1:c.417+1G=	XP_016885068.1:n.417+1G=
XM_024452390.1:c.882+1G=	XP_024308158.1:n.882+1G=
XR_001755695.1:n.1852+1G=
NM_000444.6:c.1173+1G= MANE Select	NP_000435.3:n.1173+1G=
NM_001282754.2:c.1173+1G=	NP_001269683.1:n.1173+1G=