Canonical Allele Identifier: CA2419181277

Gene: PHEX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22133446C= , CM000685.2:g.22133446C=	GRCh38
NC_000023.10:g.22151563C= , CM000685.1:g.22151563C=	GRCh37
NC_000023.9:g.22061484C=	NCBI36
NG_007563.2:g.105643C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684745.1:n.977-77C=
ENST00000379374.5:c.1303-77C= MANE Select	ENSP00000368682.4:n.1303-77C=
ENST00000379374.4:c.1303-77C=	ENSP00000368682.4:n.1303-77C=
NM_000444.5:c.1303-77C=	NP_000435.3:n.1303-77C=
NM_001282754.1:c.1303-77C=	NP_001269683.1:n.1303-77C=
XM_011545533.1:c.547-77C=	XP_011543835.1:n.547-77C=
XM_011545534.1:c.547-77C=	XP_011543836.1:n.547-77C=
XM_011545535.1:c.1303-77C=	XP_011543837.1:n.1303-77C=
XM_011545536.1:c.196-77C=	XP_011543838.1:n.196-77C=
XM_011545536.2:c.196-77C=	XP_011543838.1:n.196-77C=
XM_017029579.1:c.547-77C=	XP_016885068.1:n.547-77C=
XM_024452390.1:c.1012-77C=	XP_024308158.1:n.1012-77C=
XR_001755695.1:n.1982-77C=
NM_000444.6:c.1303-77C= MANE Select	NP_000435.3:n.1303-77C=
NM_001282754.2:c.1303-77C=	NP_001269683.1:n.1303-77C=