Canonical Allele Identifier: CA2419152396
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22047204G= , CM000685.2:g.22047204G= GRCh38
NC_000023.10:g.22065322G= , CM000685.1:g.22065322G= GRCh37
NC_000023.9:g.21975243G= NCBI36
NG_007563.2:g.19402G=

Transcript Alleles

HGVS Amino-acid change
ENST00000475778.2:n.768G=
ENST00000683214.1:n.544+14081G=
ENST00000684143.1:c.342G= ENSP00000508264.1:p.Lys114=
ENST00000379374.5:c.342G= MANE Select ENSP00000368682.4:p.Lys114=
ENST00000379374.4:c.342G= ENSP00000368682.4:p.Lys114=
NM_000444.5:c.342G= NP_000435.3:p.Lys114=
NM_001282754.1:c.342G= NP_001269683.1:p.Lys114=
XM_011545535.1:c.342G= XP_011543837.1:p.Lys114=
XM_017029579.1:c.-101G= XP_016885068.1:n.-101G=
XM_024452390.1:c.51G= XP_024308158.1:p.Lys17=
XR_001755695.1:n.1021G=
NM_000444.6:c.342G= MANE Select NP_000435.3:p.Lys114=
NM_001282754.2:c.342G= NP_001269683.1:p.Lys114=