Canonical Allele Identifier: CA2419181283

Gene: PHEX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22133472C= , CM000685.2:g.22133472C=	GRCh38
NC_000023.10:g.22151589C= , CM000685.1:g.22151589C=	GRCh37
NC_000023.9:g.22061510C=	NCBI36
NG_007563.2:g.105669C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000684745.1:n.977-51C=
ENST00000379374.5:c.1303-51C= MANE Select	ENSP00000368682.4:n.1303-51C=
ENST00000379374.4:c.1303-51C=	ENSP00000368682.4:n.1303-51C=
NM_000444.5:c.1303-51C=	NP_000435.3:n.1303-51C=
NM_001282754.1:c.1303-51C=	NP_001269683.1:n.1303-51C=
XM_011545533.1:c.547-51C=	XP_011543835.1:n.547-51C=
XM_011545534.1:c.547-51C=	XP_011543836.1:n.547-51C=
XM_011545535.1:c.1303-51C=	XP_011543837.1:n.1303-51C=
XM_011545536.1:c.196-51C=	XP_011543838.1:n.196-51C=
XM_011545536.2:c.196-51C=	XP_011543838.1:n.196-51C=
XM_017029579.1:c.547-51C=	XP_016885068.1:n.547-51C=
XM_024452390.1:c.1012-51C=	XP_024308158.1:n.1012-51C=
XR_001755695.1:n.1982-51C=
NM_000444.6:c.1303-51C= MANE Select	NP_000435.3:n.1303-51C=
NM_001282754.2:c.1303-51C=	NP_001269683.1:n.1303-51C=