Canonical Allele Identifier: CA412571382

Gene: PHEX

Linked Data

• MyVariant Identifiers: chrX:g.22095671T>A (hg19) ; chrX:g.22077553T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22077553T>A , CM000685.2:g.22077553T>A	GRCh38
NC_000023.10:g.22095671T>A , CM000685.1:g.22095671T>A	GRCh37
NC_000023.9:g.22005592T>A	NCBI36
NG_007563.2:g.49751T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000475778.2:n.940T>A
ENST00000683214.1:n.622T>A
ENST00000684143.1:c.511T>A	ENSP00000508264.1:p.Ser171Thr
ENST00000684745.1:n.188T>A
ENST00000379374.5:c.514T>A MANE Select	ENSP00000368682.4:p.Ser172Thr
ENST00000379374.4:c.514T>A	ENSP00000368682.4:p.Ser172Thr
NM_000444.5:c.514T>A	NP_000435.3:p.Ser172Thr
NM_001282754.1:c.514T>A	NP_001269683.1:p.Ser172Thr
XM_011545535.1:c.514T>A	XP_011543837.1:p.Ser172Thr
XM_017029579.1:c.-93-12876T>A	XP_016885068.1:n.-93-12876T>A
XM_024452390.1:c.223T>A	XP_024308158.1:p.Ser75Thr
XR_001755695.1:n.1193T>A
NM_000444.6:c.514T>A MANE Select	NP_000435.3:p.Ser172Thr
NM_001282754.2:c.514T>A	NP_001269683.1:p.Ser172Thr