Canonical Allele Identifier: CA327518422

Gene: PHEX

Linked Data

• dbSNP Id: rs178719
• MyVariant Identifiers: chrX:g.22064877T>C (hg19) ; chrX:g.22046759T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22046759T>C , CM000685.2:g.22046759T>C	GRCh38
NC_000023.10:g.22064877T>C , CM000685.1:g.22064877T>C	GRCh37
NC_000023.9:g.21974798T>C	NCBI36
NG_007563.2:g.18957T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.614-291T>C
ENST00000683214.1:n.544+13636T>C
ENST00000684143.1:c.188-291T>C	ENSP00000508264.1:n.188-291T>C
ENST00000379374.5:c.188-291T>C MANE Select	ENSP00000368682.4:n.188-291T>C
ENST00000379374.4:c.188-291T>C	ENSP00000368682.4:n.188-291T>C
NM_000444.5:c.188-291T>C	NP_000435.3:n.188-291T>C
NM_001282754.1:c.188-291T>C	NP_001269683.1:n.188-291T>C
XM_011545535.1:c.188-291T>C	XP_011543837.1:n.188-291T>C
XM_024452390.1:c.-104-291T>C	XP_024308158.1:n.-104-291T>C
XR_001755695.1:n.867-291T>C
NM_000444.6:c.188-291T>C MANE Select	NP_000435.3:n.188-291T>C
NM_001282754.2:c.188-291T>C	NP_001269683.1:n.188-291T>C