Canonical Allele Identifier: CA412564164

Gene: PHEX

Linked Data

• gnomAD v4: X-22033079-T-C
• MyVariant Identifiers: chrX:g.22051197T>C (hg19) ; chrX:g.22033079T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22033079T>C , CM000685.2:g.22033079T>C	GRCh38
NC_000023.10:g.22051197T>C , CM000685.1:g.22051197T>C	GRCh37
NC_000023.9:g.21961118T>C	NCBI36
NG_007563.2:g.5277T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000475778.2:n.500T>C
ENST00000683214.1:n.500T>C
ENST00000684143.1:c.74T>C	ENSP00000508264.1:p.Val25Ala
ENST00000379374.5:c.74T>C MANE Select	ENSP00000368682.4:p.Val25Ala
ENST00000379374.4:c.74T>C	ENSP00000368682.4:p.Val25Ala
NM_000444.5:c.74T>C	NP_000435.3:p.Val25Ala
NM_001282754.1:c.74T>C	NP_001269683.1:p.Val25Ala
XM_011545535.1:c.74T>C	XP_011543837.1:p.Val25Ala
XR_001755695.1:n.753T>C
NM_000444.6:c.74T>C MANE Select	NP_000435.3:p.Val25Ala
NM_001282754.2:c.74T>C	NP_001269683.1:p.Val25Ala