Canonical Allele Identifier: CA515424467

Gene: PHEX

Linked Data

• MyVariant Identifiers: chrX:g.22065271T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22047153T>C , CM000685.2:g.22047153T>C	GRCh38
NC_000023.10:g.22065271T>C , CM000685.1:g.22065271T>C	GRCh37
NC_000023.9:g.21975192T>C	NCBI36
NG_007563.2:g.19351T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.717T>C
ENST00000683214.1:n.544+14030T>C
ENST00000684143.1:c.291T>C	ENSP00000508264.1:p.Asp97=
ENST00000379374.5:c.291T>C MANE Select	ENSP00000368682.4:p.Asp97=
ENST00000379374.4:c.291T>C	ENSP00000368682.4:p.Asp97=
NM_000444.5:c.291T>C	NP_000435.3:p.Asp97=
NM_001282754.1:c.291T>C	NP_001269683.1:p.Asp97=
XM_011545535.1:c.291T>C	XP_011543837.1:p.Asp97=
XM_024452390.1:c.-1T>C	XP_024308158.1:n.-1T>C
XR_001755695.1:n.970T>C
NM_000444.6:c.291T>C MANE Select	NP_000435.3:p.Asp97=
NM_001282754.2:c.291T>C	NP_001269683.1:p.Asp97=