Canonical Allele Identifier: CA2693304211
Gene: PHEX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22047037dup , CM000685.2:g.22047037dup GRCh38
NC_000023.10:g.22065155dup , CM000685.1:g.22065155dup GRCh37
NC_000023.9:g.21975076dup NCBI36
NG_007563.2:g.19235dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000475778.2:n.614-13dup
ENST00000683214.1:n.544+13914dup
ENST00000684143.1:c.188-13dup ENSP00000508264.1:n.188-13dup
ENST00000379374.5:c.188-13dup MANE Select ENSP00000368682.4:n.188-13dup
ENST00000379374.4:c.188-13dup ENSP00000368682.4:n.188-13dup
NM_000444.5:c.188-13dup NP_000435.3:n.188-13dup
NM_001282754.1:c.188-13dup NP_001269683.1:n.188-13dup
XM_011545535.1:c.188-13dup XP_011543837.1:n.188-13dup
XM_024452390.1:c.-104-13dup XP_024308158.1:n.-104-13dup
XR_001755695.1:n.867-13dup
NM_000444.6:c.188-13dup MANE Select NP_000435.3:n.188-13dup
NM_001282754.2:c.188-13dup NP_001269683.1:n.188-13dup