Canonical Allele Identifier: CA515423637

Gene: PHEX

Linked Data

• MyVariant Identifiers: chrX:g.22112106G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22093988G>C , CM000685.2:g.22093988G>C	GRCh38
NC_000023.10:g.22112106G>C , CM000685.1:g.22112106G>C	GRCh37
NC_000023.9:g.22022027G>C	NCBI36
NG_007563.2:g.66186G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.1164G>C
ENST00000684143.1:c.735G>C	ENSP00000508264.1:p.Arg245=
ENST00000684745.1:n.412G>C
ENST00000379374.5:c.738G>C MANE Select	ENSP00000368682.4:p.Arg246=
ENST00000379374.4:c.738G>C	ENSP00000368682.4:p.Arg246=
ENST00000475778.1:n.11G>C
NM_000444.5:c.738G>C	NP_000435.3:p.Arg246=
NM_001282754.1:c.738G>C	NP_001269683.1:p.Arg246=
XM_011545533.1:c.-19G>C	XP_011543835.1:n.-19G>C
XM_011545534.1:c.-19G>C	XP_011543836.1:n.-19G>C
XM_011545535.1:c.738G>C	XP_011543837.1:p.Arg246=
XM_017029579.1:c.-19G>C	XP_016885068.1:n.-19G>C
XM_024452390.1:c.447G>C	XP_024308158.1:p.Arg149=
XR_001755695.1:n.1417G>C
NM_000444.6:c.738G>C MANE Select	NP_000435.3:p.Arg246=
NM_001282754.2:c.738G>C	NP_001269683.1:p.Arg246=