Canonical Allele Identifier: CA2419168518

Gene: PHEX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22096795C= , CM000685.2:g.22096795C=	GRCh38
NC_000023.10:g.22114913C= , CM000685.1:g.22114913C=	GRCh37
NC_000023.9:g.22024834C=	NCBI36
NG_007563.2:g.68993C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.1276-160C=
ENST00000684143.1:c.847-160C=	ENSP00000508264.1:n.847-160C=
ENST00000684745.1:n.524-160C=
ENST00000379374.5:c.850-160C= MANE Select	ENSP00000368682.4:n.850-160C=
ENST00000379374.4:c.850-160C=	ENSP00000368682.4:n.850-160C=
ENST00000475778.1:n.123-160C=
NM_000444.5:c.850-160C=	NP_000435.3:n.850-160C=
NM_001282754.1:c.850-160C=	NP_001269683.1:n.850-160C=
XM_011545533.1:c.94-160C=	XP_011543835.1:n.94-160C=
XM_011545534.1:c.94-160C=	XP_011543836.1:n.94-160C=
XM_011545535.1:c.850-160C=	XP_011543837.1:n.850-160C=
XM_017029579.1:c.94-160C=	XP_016885068.1:n.94-160C=
XM_024452390.1:c.559-160C=	XP_024308158.1:n.559-160C=
XR_001755695.1:n.1529-160C=
NM_000444.6:c.850-160C= MANE Select	NP_000435.3:n.850-160C=
NM_001282754.2:c.850-160C=	NP_001269683.1:n.850-160C=