Canonical Allele Identifier: CA412574590
Community Standard Title: NM_000444.6(PHEX):c.1331G>A (p.Trp444Ter)
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22133551G>A , CM000685.2:g.22133551G>A GRCh38
NC_000023.10:g.22151668G>A , CM000685.1:g.22151668G>A GRCh37
NC_000023.9:g.22061589G>A NCBI36
NG_007563.2:g.105748G>A

Transcript Alleles

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