Canonical Allele Identifier: CA2419152349
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22047088C= , CM000685.2:g.22047088C= GRCh38
NC_000023.10:g.22065206C= , CM000685.1:g.22065206C= GRCh37
NC_000023.9:g.21975127C= NCBI36
NG_007563.2:g.19286C=

Transcript Alleles

HGVS Amino-acid change
ENST00000475778.2:n.652C=
ENST00000683214.1:n.544+13965C=
ENST00000684143.1:c.226C= ENSP00000508264.1:p.Pro76=
ENST00000379374.5:c.226C= MANE Select ENSP00000368682.4:p.Pro76=
ENST00000379374.4:c.226C= ENSP00000368682.4:p.Pro76=
NM_000444.5:c.226C= NP_000435.3:p.Pro76=
NM_001282754.1:c.226C= NP_001269683.1:p.Pro76=
XM_011545535.1:c.226C= XP_011543837.1:p.Pro76=
XM_024452390.1:c.-66C= XP_024308158.1:n.-66C=
XR_001755695.1:n.905C=
NM_000444.6:c.226C= MANE Select NP_000435.3:p.Pro76=
NM_001282754.2:c.226C= NP_001269683.1:p.Pro76=