Canonical Allele Identifier: CA2419168578

Gene: PHEX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22096943T= , CM000685.2:g.22096943T=	GRCh38
NC_000023.10:g.22115061T= , CM000685.1:g.22115061T=	GRCh37
NC_000023.9:g.22024982T=	NCBI36
NG_007563.2:g.69141T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000475778.2:n.1276-12T=
ENST00000684143.1:c.847-12T=	ENSP00000508264.1:n.847-12T=
ENST00000684745.1:n.524-12T=
ENST00000379374.5:c.850-12T= MANE Select	ENSP00000368682.4:n.850-12T=
ENST00000379374.4:c.850-12T=	ENSP00000368682.4:n.850-12T=
ENST00000475778.1:n.123-12T=
NM_000444.5:c.850-12T=	NP_000435.3:n.850-12T=
NM_001282754.1:c.850-12T=	NP_001269683.1:n.850-12T=
XM_011545533.1:c.94-12T=	XP_011543835.1:n.94-12T=
XM_011545534.1:c.94-12T=	XP_011543836.1:n.94-12T=
XM_011545535.1:c.850-12T=	XP_011543837.1:n.850-12T=
XM_017029579.1:c.94-12T=	XP_016885068.1:n.94-12T=
XM_024452390.1:c.559-12T=	XP_024308158.1:n.559-12T=
XR_001755695.1:n.1529-12T=
NM_000444.6:c.850-12T= MANE Select	NP_000435.3:n.850-12T=
NM_001282754.2:c.850-12T=	NP_001269683.1:n.850-12T=