Canonical Allele Identifier: CA412568157
Gene: PHEX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22047208A>G , CM000685.2:g.22047208A>G GRCh38
NC_000023.10:g.22065326A>G , CM000685.1:g.22065326A>G GRCh37
NC_000023.9:g.21975247A>G NCBI36
NG_007563.2:g.19406A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000475778.2:n.772A>G
ENST00000683214.1:n.544+14085A>G
ENST00000684143.1:c.346A>G ENSP00000508264.1:p.Lys116Glu
ENST00000379374.5:c.346A>G MANE Select ENSP00000368682.4:p.Lys116Glu
ENST00000379374.4:c.346A>G ENSP00000368682.4:p.Lys116Glu
NM_000444.5:c.346A>G NP_000435.3:p.Lys116Glu
NM_001282754.1:c.346A>G NP_001269683.1:p.Lys116Glu
XM_011545535.1:c.346A>G XP_011543837.1:p.Lys116Glu
XM_017029579.1:c.-97A>G XP_016885068.1:n.-97A>G
XM_024452390.1:c.55A>G XP_024308158.1:p.Lys19Glu
XR_001755695.1:n.1025A>G
NM_000444.6:c.346A>G MANE Select NP_000435.3:p.Lys116Glu
NM_001282754.2:c.346A>G NP_001269683.1:p.Lys116Glu