Canonical Allele Identifier: CA412571661

Gene: PHEX

Linked Data

• dbSNP Id: rs1929217955
• MyVariant Identifiers: chrX:g.22095797G>C (hg19) ; chrX:g.22077679G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22077679G>C , CM000685.2:g.22077679G>C	GRCh38
NC_000023.10:g.22095797G>C , CM000685.1:g.22095797G>C	GRCh37
NC_000023.9:g.22005718G>C	NCBI36
NG_007563.2:g.49877G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.1066G>C
ENST00000683214.1:n.748G>C
ENST00000684143.1:c.637G>C	ENSP00000508264.1:p.Ala213Pro
ENST00000684745.1:n.314G>C
ENST00000379374.5:c.640G>C MANE Select	ENSP00000368682.4:p.Ala214Pro
ENST00000379374.4:c.640G>C	ENSP00000368682.4:p.Ala214Pro
NM_000444.5:c.640G>C	NP_000435.3:p.Ala214Pro
NM_001282754.1:c.640G>C	NP_001269683.1:p.Ala214Pro
XM_011545535.1:c.640G>C	XP_011543837.1:p.Ala214Pro
XM_017029579.1:c.-93-12750G>C	XP_016885068.1:n.-93-12750G>C
XM_024452390.1:c.349G>C	XP_024308158.1:p.Ala117Pro
XR_001755695.1:n.1319G>C
NM_000444.6:c.640G>C MANE Select	NP_000435.3:p.Ala214Pro
NM_001282754.2:c.640G>C	NP_001269683.1:p.Ala214Pro