Canonical Allele Identifier: CA412567767
Gene: PHEX HGNC NCBI

Linked Data

ClinVar Variation Id: 426473
ClinVar RCV Id: RCV000490200
dbSNP Id: rs1085307642

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22047174T>G , CM000685.2:g.22047174T>G GRCh38
NC_000023.10:g.22065292T>G , CM000685.1:g.22065292T>G GRCh37
NC_000023.9:g.21975213T>G NCBI36
NG_007563.2:g.19372T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000475778.2:n.738T>G
ENST00000683214.1:n.544+14051T>G
ENST00000684143.1:c.312T>G ENSP00000508264.1:p.Tyr104Ter
ENST00000379374.5:c.312T>G MANE Select ENSP00000368682.4:p.Tyr104Ter
ENST00000379374.4:c.312T>G ENSP00000368682.4:p.Tyr104Ter
NM_000444.5:c.312T>G NP_000435.3:p.Tyr104Ter
NM_001282754.1:c.312T>G NP_001269683.1:p.Tyr104Ter
XM_011545535.1:c.312T>G XP_011543837.1:p.Tyr104Ter
XM_024452390.1:c.21T>G XP_024308158.1:p.Tyr7Ter
XR_001755695.1:n.991T>G
NM_000444.6:c.312T>G MANE Select NP_000435.3:p.Tyr104Ter
NM_001282754.2:c.312T>G NP_001269683.1:p.Tyr104Ter