Canonical Allele Identifier: CA412568094

Gene: PHEX

Linked Data

• gnomAD v4: X-22047194-T-C
• MyVariant Identifiers: chrX:g.22065312T>C (hg19) ; chrX:g.22047194T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22047194T>C , CM000685.2:g.22047194T>C	GRCh38
NC_000023.10:g.22065312T>C , CM000685.1:g.22065312T>C	GRCh37
NC_000023.9:g.21975233T>C	NCBI36
NG_007563.2:g.19392T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000475778.2:n.758T>C
ENST00000683214.1:n.544+14071T>C
ENST00000684143.1:c.332T>C	ENSP00000508264.1:p.Val111Ala
ENST00000379374.5:c.332T>C MANE Select	ENSP00000368682.4:p.Val111Ala
ENST00000379374.4:c.332T>C	ENSP00000368682.4:p.Val111Ala
NM_000444.5:c.332T>C	NP_000435.3:p.Val111Ala
NM_001282754.1:c.332T>C	NP_001269683.1:p.Val111Ala
XM_011545535.1:c.332T>C	XP_011543837.1:p.Val111Ala
XM_017029579.1:c.-111T>C	XP_016885068.1:n.-111T>C
XM_024452390.1:c.41T>C	XP_024308158.1:p.Val14Ala
XR_001755695.1:n.1011T>C
NM_000444.6:c.332T>C MANE Select	NP_000435.3:p.Val111Ala
NM_001282754.2:c.332T>C	NP_001269683.1:p.Val111Ala