Canonical Allele Identifier: CA2419195609
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22178385_22178389delinsTAAAC , CM000685.2:g.22178385_22178389delinsTAAAC GRCh38
NC_000023.10:g.22196502_22196506delinsTAAAC , CM000685.1:g.22196502_22196506delinsTAAAC GRCh37
NC_000023.9:g.22106423_22106427delinsTAAAC NCBI36
NG_007563.2:g.150582_150586delinsTAAAC

Transcript Alleles

HGVS Amino-acid change
ENST00000682888.1:c.140+9_140+13delinsTAAAC ENSP00000508003.1:n.140+9_140+13delinsTAA...
ENST00000683162.1:c.140+9_140+13delinsTAAAC ENSP00000508059.1:n.140+9_140+13delinsTAA...
ENST00000683289.1:c.140+9_140+13delinsTAAAC ENSP00000508195.1:n.140+9_140+13delinsTAA...
ENST00000683917.1:n.370+9_370+13delinsTAAAC
ENST00000684356.1:c.140+9_140+13delinsTAAAC ENSP00000507619.1:n.140+9_140+13delinsTAA...
ENST00000684745.1:n.1260+9_1260+13delinsTAAAC
ENST00000379374.5:c.1586+9_1586+13delinsTAAAC MANE Select ENSP00000368682.4:n.1586+9_1586+13delinsT...
ENST00000379374.4:c.1586+9_1586+13delinsTAAAC ENSP00000368682.4:n.1586+9_1586+13delinsT...
NM_000444.5:c.1586+9_1586+13delinsTAAAC NP_000435.3:n.1586+9_1586+13delinsTAAAC
NM_001282754.1:c.1586+9_1586+13delinsTAAAC NP_001269683.1:n.1586+9_1586+13delinsTAAA...
XM_011545533.1:c.830+9_830+13delinsTAAAC XP_011543835.1:n.830+9_830+13delinsTAAAC
XM_011545534.1:c.830+9_830+13delinsTAAAC XP_011543836.1:n.830+9_830+13delinsTAAAC
XM_011545536.1:c.479+9_479+13delinsTAAAC XP_011543838.1:n.479+9_479+13delinsTAAAC
XM_011545536.2:c.479+9_479+13delinsTAAAC XP_011543838.1:n.479+9_479+13delinsTAAAC
XM_017029579.1:c.830+9_830+13delinsTAAAC XP_016885068.1:n.830+9_830+13delinsTAAAC
XM_024452390.1:c.1295+9_1295+13delinsTAAAC XP_024308158.1:n.1295+9_1295+13delinsTAAA...
XR_001755695.1:n.2426+9_2426+13delinsTAAAC
NM_000444.6:c.1586+9_1586+13delinsTAAAC MANE Select NP_000435.3:n.1586+9_1586+13delinsTAAAC
NM_001282754.2:c.1586+9_1586+13delinsTAAAC NP_001269683.1:n.1586+9_1586+13delinsTAAA...