Canonical Allele Identifier: CA2419168541

Gene: PHEX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22096846C= , CM000685.2:g.22096846C=	GRCh38
NC_000023.10:g.22114964C= , CM000685.1:g.22114964C=	GRCh37
NC_000023.9:g.22024885C=	NCBI36
NG_007563.2:g.69044C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.1276-109C=
ENST00000684143.1:c.847-109C=	ENSP00000508264.1:n.847-109C=
ENST00000684745.1:n.524-109C=
ENST00000379374.5:c.850-109C= MANE Select	ENSP00000368682.4:n.850-109C=
ENST00000379374.4:c.850-109C=	ENSP00000368682.4:n.850-109C=
ENST00000475778.1:n.123-109C=
NM_000444.5:c.850-109C=	NP_000435.3:n.850-109C=
NM_001282754.1:c.850-109C=	NP_001269683.1:n.850-109C=
XM_011545533.1:c.94-109C=	XP_011543835.1:n.94-109C=
XM_011545534.1:c.94-109C=	XP_011543836.1:n.94-109C=
XM_011545535.1:c.850-109C=	XP_011543837.1:n.850-109C=
XM_017029579.1:c.94-109C=	XP_016885068.1:n.94-109C=
XM_024452390.1:c.559-109C=	XP_024308158.1:n.559-109C=
XR_001755695.1:n.1529-109C=
NM_000444.6:c.850-109C= MANE Select	NP_000435.3:n.850-109C=
NM_001282754.2:c.850-109C=	NP_001269683.1:n.850-109C=