Canonical Allele Identifier: CA2579571845
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22047220C>T , CM000685.2:g.22047220C>T GRCh38
NC_000023.10:g.22065338C>T , CM000685.1:g.22065338C>T GRCh37
NC_000023.9:g.21975259C>T NCBI36
NG_007563.2:g.19418C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000475778.2:n.775+9C>T
ENST00000683214.1:n.544+14097C>T
ENST00000684143.1:c.349+9C>T ENSP00000508264.1:n.349+9C>T
ENST00000379374.5:c.349+9C>T MANE Select ENSP00000368682.4:n.349+9C>T
ENST00000379374.4:c.349+9C>T ENSP00000368682.4:n.349+9C>T
NM_000444.5:c.349+9C>T NP_000435.3:n.349+9C>T
NM_001282754.1:c.349+9C>T NP_001269683.1:n.349+9C>T
XM_011545535.1:c.349+9C>T XP_011543837.1:n.349+9C>T
XM_017029579.1:c.-94+9C>T XP_016885068.1:n.-94+9C>T
XM_024452390.1:c.58+9C>T XP_024308158.1:n.58+9C>T
XR_001755695.1:n.1028+9C>T
NM_000444.6:c.349+9C>T MANE Select NP_000435.3:n.349+9C>T
NM_001282754.2:c.349+9C>T NP_001269683.1:n.349+9C>T