Canonical Allele Identifier: CA412567677

Gene: PHEX

Linked Data

• MyVariant Identifiers: chrX:g.22065252A>T (hg19) ; chrX:g.22047134A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22047134A>T , CM000685.2:g.22047134A>T	GRCh38
NC_000023.10:g.22065252A>T , CM000685.1:g.22065252A>T	GRCh37
NC_000023.9:g.21975173A>T	NCBI36
NG_007563.2:g.19332A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.698A>T
ENST00000683214.1:n.544+14011A>T
ENST00000684143.1:c.272A>T	ENSP00000508264.1:p.Asn91Ile
ENST00000379374.5:c.272A>T MANE Select	ENSP00000368682.4:p.Asn91Ile
ENST00000379374.4:c.272A>T	ENSP00000368682.4:p.Asn91Ile
NM_000444.5:c.272A>T	NP_000435.3:p.Asn91Ile
NM_001282754.1:c.272A>T	NP_001269683.1:p.Asn91Ile
XM_011545535.1:c.272A>T	XP_011543837.1:p.Asn91Ile
XM_024452390.1:c.-20A>T	XP_024308158.1:n.-20A>T
XR_001755695.1:n.951A>T
NM_000444.6:c.272A>T MANE Select	NP_000435.3:p.Asn91Ile
NM_001282754.2:c.272A>T	NP_001269683.1:p.Asn91Ile