Canonical Allele Identifier: CA2695231781

Gene: PHEX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22133551_22133552insAAC , CM000685.2:g.22133551_22133552insAAC	GRCh38
NC_000023.10:g.22151668_22151669insAAC , CM000685.1:g.22151668_22151669insAAC	GRCh37
NC_000023.9:g.22061589_22061590insAAC	NCBI36
NG_007563.2:g.105748_105749insAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684745.1:n.1005_1006insAAC
ENST00000379374.5:c.1331_1332insAAC MANE Select	ENSP00000368682.4:p.Trp444Ter
ENST00000379374.4:c.1331_1332insAAC	ENSP00000368682.4:p.Trp444Ter
NM_000444.5:c.1331_1332insAAC	NP_000435.3:p.Trp444Ter
NM_001282754.1:c.1331_1332insAAC	NP_001269683.1:p.Trp444Ter
XM_011545533.1:c.575_576insAAC	XP_011543835.1:p.Trp192Ter
XM_011545534.1:c.575_576insAAC	XP_011543836.1:p.Trp192Ter
XM_011545535.1:c.1331_1332insAAC	XP_011543837.1:p.Trp444Ter
XM_011545536.1:c.224_225insAAC	XP_011543838.1:p.Trp75Ter
XM_011545536.2:c.224_225insAAC	XP_011543838.1:p.Trp75Ter
XM_017029579.1:c.575_576insAAC	XP_016885068.1:p.Trp192Ter
XM_024452390.1:c.1040_1041insAAC	XP_024308158.1:p.Trp347Ter
XR_001755695.1:n.2010_2011insAAC
NM_000444.6:c.1331_1332insAAC MANE Select	NP_000435.3:p.Trp444Ter
NM_001282754.2:c.1331_1332insAAC	NP_001269683.1:p.Trp444Ter