Canonical Allele Identifier: CA412571608

Gene: PHEX

Linked Data

• MyVariant Identifiers: chrX:g.22095771G>C (hg19) ; chrX:g.22077653G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22077653G>C , CM000685.2:g.22077653G>C	GRCh38
NC_000023.10:g.22095771G>C , CM000685.1:g.22095771G>C	GRCh37
NC_000023.9:g.22005692G>C	NCBI36
NG_007563.2:g.49851G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000475778.2:n.1040G>C
ENST00000683214.1:n.722G>C
ENST00000684143.1:c.611G>C	ENSP00000508264.1:p.Arg204Pro
ENST00000684745.1:n.288G>C
ENST00000379374.5:c.614G>C MANE Select	ENSP00000368682.4:p.Arg205Pro
ENST00000379374.4:c.614G>C	ENSP00000368682.4:p.Arg205Pro
NM_000444.5:c.614G>C	NP_000435.3:p.Arg205Pro
NM_001282754.1:c.614G>C	NP_001269683.1:p.Arg205Pro
XM_011545535.1:c.614G>C	XP_011543837.1:p.Arg205Pro
XM_017029579.1:c.-93-12776G>C	XP_016885068.1:n.-93-12776G>C
XM_024452390.1:c.323G>C	XP_024308158.1:p.Arg108Pro
XR_001755695.1:n.1293G>C
NM_000444.6:c.614G>C MANE Select	NP_000435.3:p.Arg205Pro
NM_001282754.2:c.614G>C	NP_001269683.1:p.Arg205Pro