Canonical Allele Identifier: CA412574868

Gene: PHEX

Linked Data

• MyVariant Identifiers: chrX:g.22196431A>T (hg19) ; chrX:g.22178314A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22178314A>T , CM000685.2:g.22178314A>T	GRCh38
NC_000023.10:g.22196431A>T , CM000685.1:g.22196431A>T	GRCh37
NC_000023.9:g.22106352A>T	NCBI36
NG_007563.2:g.150511A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682888.1:c.78A>T	ENSP00000508003.1:p.Gln26His
ENST00000683162.1:c.78A>T	ENSP00000508059.1:p.Gln26His
ENST00000683289.1:c.78A>T	ENSP00000508195.1:p.Gln26His
ENST00000683917.1:n.308A>T
ENST00000684356.1:c.78A>T	ENSP00000507619.1:p.Gln26His
ENST00000684745.1:n.1198A>T
ENST00000379374.5:c.1524A>T MANE Select	ENSP00000368682.4:p.Gln508His
ENST00000379374.4:c.1524A>T	ENSP00000368682.4:p.Gln508His
NM_000444.5:c.1524A>T	NP_000435.3:p.Gln508His
NM_001282754.1:c.1524A>T	NP_001269683.1:p.Gln508His
XM_011545533.1:c.768A>T	XP_011543835.1:p.Gln256His
XM_011545534.1:c.768A>T	XP_011543836.1:p.Gln256His
XM_011545536.1:c.417A>T	XP_011543838.1:p.Gln139His
XM_011545536.2:c.417A>T	XP_011543838.1:p.Gln139His
XM_017029579.1:c.768A>T	XP_016885068.1:p.Gln256His
XM_024452390.1:c.1233A>T	XP_024308158.1:p.Gln411His
XR_001755695.1:n.2364A>T
NM_000444.6:c.1524A>T MANE Select	NP_000435.3:p.Gln508His
NM_001282754.2:c.1524A>T	NP_001269683.1:p.Gln508His