Canonical Allele Identifier: CA2419152395
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22047191_22047194delinsATGT , CM000685.2:g.22047191_22047194delinsATGT GRCh38
NC_000023.10:g.22065309_22065312delinsATGT , CM000685.1:g.22065309_22065312delinsATGT GRCh37
NC_000023.9:g.21975230_21975233delinsATGT NCBI36
NG_007563.2:g.19389_19392delinsATGT

Transcript Alleles

HGVS Amino-acid change
ENST00000475778.2:n.755_758delinsATGT
ENST00000683214.1:n.544+14068_544+14071delinsATGT
ENST00000684143.1:c.329_332delinsATGT ENSP00000508264.1:p.Asn110=
ENST00000379374.5:c.329_332delinsATGT MANE Select ENSP00000368682.4:p.Asn110=
ENST00000379374.4:c.329_332delinsATGT ENSP00000368682.4:p.Asn110=
NM_000444.5:c.329_332delinsATGT NP_000435.3:p.Asn110=
NM_001282754.1:c.329_332delinsATGT NP_001269683.1:p.Asn110=
XM_011545535.1:c.329_332delinsATGT XP_011543837.1:p.Asn110=
XM_017029579.1:c.-114_-111delinsATGT XP_016885068.1:n.-114_-111delinsATGT
XM_024452390.1:c.38_41delinsATGT XP_024308158.1:p.Asn13=
XR_001755695.1:n.1008_1011delinsATGT
NM_000444.6:c.329_332delinsATGT MANE Select NP_000435.3:p.Asn110=
NM_001282754.2:c.329_332delinsATGT NP_001269683.1:p.Asn110=