Canonical Allele Identifier: CA2693304831
Gene: PHEX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22096840_22096841dup , CM000685.2:g.22096840_22096841dup GRCh38
NC_000023.10:g.22114958_22114959dup , CM000685.1:g.22114958_22114959dup GRCh37
NC_000023.9:g.22024879_22024880dup NCBI36
NG_007563.2:g.69038_69039dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000475778.2:n.1276-115_1276-114dup
ENST00000684143.1:c.847-115_847-114dup ENSP00000508264.1:n.847-115_847-114dup
ENST00000684745.1:n.524-115_524-114dup
ENST00000379374.5:c.850-115_850-114dup MANE Select ENSP00000368682.4:n.850-115_850-114dup
ENST00000379374.4:c.850-115_850-114dup ENSP00000368682.4:n.850-115_850-114dup
ENST00000475778.1:n.123-115_123-114dup
NM_000444.5:c.850-115_850-114dup NP_000435.3:n.850-115_850-114dup
NM_001282754.1:c.850-115_850-114dup NP_001269683.1:n.850-115_850-114dup
XM_011545533.1:c.94-115_94-114dup XP_011543835.1:n.94-115_94-114dup
XM_011545534.1:c.94-115_94-114dup XP_011543836.1:n.94-115_94-114dup
XM_011545535.1:c.850-115_850-114dup XP_011543837.1:n.850-115_850-114dup
XM_017029579.1:c.94-115_94-114dup XP_016885068.1:n.94-115_94-114dup
XM_024452390.1:c.559-115_559-114dup XP_024308158.1:n.559-115_559-114dup
XR_001755695.1:n.1529-115_1529-114dup
NM_000444.6:c.850-115_850-114dup MANE Select NP_000435.3:n.850-115_850-114dup
NM_001282754.2:c.850-115_850-114dup NP_001269683.1:n.850-115_850-114dup