Canonical Allele Identifier: CA412574762

Gene: PHEX

Linked Data

• MyVariant Identifiers: chrX:g.22151730G>T (hg19) ; chrX:g.22133613G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22133613G>T , CM000685.2:g.22133613G>T	GRCh38
NC_000023.10:g.22151730G>T , CM000685.1:g.22151730G>T	GRCh37
NC_000023.9:g.22061651G>T	NCBI36
NG_007563.2:g.105810G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684745.1:n.1067G>T
ENST00000379374.5:c.1393G>T MANE Select	ENSP00000368682.4:p.Ala465Ser
ENST00000379374.4:c.1393G>T	ENSP00000368682.4:p.Ala465Ser
NM_000444.5:c.1393G>T	NP_000435.3:p.Ala465Ser
NM_001282754.1:c.1393G>T	NP_001269683.1:p.Ala465Ser
XM_011545533.1:c.637G>T	XP_011543835.1:p.Ala213Ser
XM_011545534.1:c.637G>T	XP_011543836.1:p.Ala213Ser
XM_011545535.1:c.1393G>T	XP_011543837.1:p.Ala465Ser
XM_011545536.1:c.286G>T	XP_011543838.1:p.Ala96Ser
XM_011545536.2:c.286G>T	XP_011543838.1:p.Ala96Ser
XM_017029579.1:c.637G>T	XP_016885068.1:p.Ala213Ser
XM_024452390.1:c.1102G>T	XP_024308158.1:p.Ala368Ser
XR_001755695.1:n.2072G>T
NM_000444.6:c.1393G>T MANE Select	NP_000435.3:p.Ala465Ser
NM_001282754.2:c.1393G>T	NP_001269683.1:p.Ala465Ser