Canonical Allele Identifier: CA515427390

Gene: PHEX

Linked Data

• MyVariant Identifiers: chrX:g.22151663T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22133546T>A , CM000685.2:g.22133546T>A	GRCh38
NC_000023.10:g.22151663T>A , CM000685.1:g.22151663T>A	GRCh37
NC_000023.9:g.22061584T>A	NCBI36
NG_007563.2:g.105743T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000684745.1:n.1000T>A
ENST00000379374.5:c.1326T>A MANE Select	ENSP00000368682.4:p.Val442=
ENST00000379374.4:c.1326T>A	ENSP00000368682.4:p.Val442=
NM_000444.5:c.1326T>A	NP_000435.3:p.Val442=
NM_001282754.1:c.1326T>A	NP_001269683.1:p.Val442=
XM_011545533.1:c.570T>A	XP_011543835.1:p.Val190=
XM_011545534.1:c.570T>A	XP_011543836.1:p.Val190=
XM_011545535.1:c.1326T>A	XP_011543837.1:p.Val442=
XM_011545536.1:c.219T>A	XP_011543838.1:p.Val73=
XM_011545536.2:c.219T>A	XP_011543838.1:p.Val73=
XM_017029579.1:c.570T>A	XP_016885068.1:p.Val190=
XM_024452390.1:c.1035T>A	XP_024308158.1:p.Val345=
XR_001755695.1:n.2005T>A
NM_000444.6:c.1326T>A MANE Select	NP_000435.3:p.Val442=
NM_001282754.2:c.1326T>A	NP_001269683.1:p.Val442=