Canonical Allele Identifier: CA2738437115
Gene: PHEX HGNC NCBI

Linked Data

dbSNP Id: rs2146987573

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22046977del , CM000685.2:g.22046977del GRCh38
NC_000023.10:g.22065095del , CM000685.1:g.22065095del GRCh37
NC_000023.9:g.21975016del NCBI36
NG_007563.2:g.19175del

Transcript Alleles

HGVS Amino-acid Change
ENST00000475778.2:n.614-73del
ENST00000683214.1:n.544+13854del
ENST00000684143.1:c.188-73del ENSP00000508264.1:n.188-73del
ENST00000379374.5:c.188-73del MANE Select ENSP00000368682.4:n.188-73del
ENST00000379374.4:c.188-73del ENSP00000368682.4:n.188-73del
NM_000444.5:c.188-73del NP_000435.3:n.188-73del
NM_001282754.1:c.188-73del NP_001269683.1:n.188-73del
XM_011545535.1:c.188-73del XP_011543837.1:n.188-73del
XM_024452390.1:c.-104-73del XP_024308158.1:n.-104-73del
XR_001755695.1:n.867-73del
NM_000444.6:c.188-73del MANE Select NP_000435.3:n.188-73del
NM_001282754.2:c.188-73del NP_001269683.1:n.188-73del