Canonical Allele Identifier: CA2419195646

Gene: PHEX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22178515G= , CM000685.2:g.22178515G=	GRCh38
NC_000023.10:g.22196632G= , CM000685.1:g.22196632G=	GRCh37
NC_000023.9:g.22106553G=	NCBI36
NG_007563.2:g.150712G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682888.1:c.140+139G=	ENSP00000508003.1:n.140+139G=
ENST00000683162.1:c.140+139G=	ENSP00000508059.1:n.140+139G=
ENST00000683289.1:c.140+139G=	ENSP00000508195.1:n.140+139G=
ENST00000683917.1:n.370+139G=
ENST00000684356.1:c.140+139G=	ENSP00000507619.1:n.140+139G=
ENST00000684745.1:n.1260+139G=
ENST00000379374.5:c.1586+139G= MANE Select	ENSP00000368682.4:n.1586+139G=
ENST00000379374.4:c.1586+139G=	ENSP00000368682.4:n.1586+139G=
NM_000444.5:c.1586+139G=	NP_000435.3:n.1586+139G=
NM_001282754.1:c.1586+139G=	NP_001269683.1:n.1586+139G=
XM_011545533.1:c.830+139G=	XP_011543835.1:n.830+139G=
XM_011545534.1:c.830+139G=	XP_011543836.1:n.830+139G=
XM_011545536.1:c.479+139G=	XP_011543838.1:n.479+139G=
XM_011545536.2:c.479+139G=	XP_011543838.1:n.479+139G=
XM_017029579.1:c.830+139G=	XP_016885068.1:n.830+139G=
XM_024452390.1:c.1295+139G=	XP_024308158.1:n.1295+139G=
XR_001755695.1:n.2426+139G=
NM_000444.6:c.1586+139G= MANE Select	NP_000435.3:n.1586+139G=
NM_001282754.2:c.1586+139G=	NP_001269683.1:n.1586+139G=