Canonical Allele Identifier: CA2579571833
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22046967A>T , CM000685.2:g.22046967A>T GRCh38
NC_000023.10:g.22065085A>T , CM000685.1:g.22065085A>T GRCh37
NC_000023.9:g.21975006A>T NCBI36
NG_007563.2:g.19165A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000475778.2:n.614-83A>T
ENST00000683214.1:n.544+13844A>T
ENST00000684143.1:c.188-83A>T ENSP00000508264.1:n.188-83A>T
ENST00000379374.5:c.188-83A>T MANE Select ENSP00000368682.4:n.188-83A>T
ENST00000379374.4:c.188-83A>T ENSP00000368682.4:n.188-83A>T
NM_000444.5:c.188-83A>T NP_000435.3:n.188-83A>T
NM_001282754.1:c.188-83A>T NP_001269683.1:n.188-83A>T
XM_011545535.1:c.188-83A>T XP_011543837.1:n.188-83A>T
XM_024452390.1:c.-104-83A>T XP_024308158.1:n.-104-83A>T
XR_001755695.1:n.867-83A>T
NM_000444.6:c.188-83A>T MANE Select NP_000435.3:n.188-83A>T
NM_001282754.2:c.188-83A>T NP_001269683.1:n.188-83A>T