Canonical Allele Identifier: CA412567743

Gene: PHEX

Linked Data

• MyVariant Identifiers: chrX:g.22065281T>G (hg19) ; chrX:g.22047163T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22047163T>G , CM000685.2:g.22047163T>G	GRCh38
NC_000023.10:g.22065281T>G , CM000685.1:g.22065281T>G	GRCh37
NC_000023.9:g.21975202T>G	NCBI36
NG_007563.2:g.19361T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.727T>G
ENST00000683214.1:n.544+14040T>G
ENST00000684143.1:c.301T>G	ENSP00000508264.1:p.Tyr101Asp
ENST00000379374.5:c.301T>G MANE Select	ENSP00000368682.4:p.Tyr101Asp
ENST00000379374.4:c.301T>G	ENSP00000368682.4:p.Tyr101Asp
NM_000444.5:c.301T>G	NP_000435.3:p.Tyr101Asp
NM_001282754.1:c.301T>G	NP_001269683.1:p.Tyr101Asp
XM_011545535.1:c.301T>G	XP_011543837.1:p.Tyr101Asp
XM_024452390.1:c.10T>G	XP_024308158.1:p.Tyr4Asp
XR_001755695.1:n.980T>G
NM_000444.6:c.301T>G MANE Select	NP_000435.3:p.Tyr101Asp
NM_001282754.2:c.301T>G	NP_001269683.1:p.Tyr101Asp