Canonical Allele Identifier: CA412564713
Community Standard Title: NM_000444.6(PHEX):c.119-1G>A
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22038468G>A , CM000685.2:g.22038468G>A GRCh38
NC_000023.10:g.22056586G>A , CM000685.1:g.22056586G>A GRCh37
NC_000023.9:g.21966507G>A NCBI36
NG_007563.2:g.10666G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000444.6:c.119-1G>A MANE Select NP_000435.3:n.119-1G>A
ENST00000379374.5:c.119-1G>A MANE Select ENSP00000368682.4:n.119-1G>A
NM_000444.5:c.119-1G>A NP_000435.3:n.119-1G>A
NM_001282754.1:c.119-1G>A NP_001269683.1:n.119-1G>A
NM_001282754.2:c.119-1G>A NP_001269683.1:n.119-1G>A
ENST00000379374.4:c.119-1G>A ENSP00000368682.4:n.119-1G>A
ENST00000475778.2:n.545-1G>A
ENST00000683214.1:n.544+5345G>A
ENST00000684143.1:c.119-1G>A ENSP00000508264.1:n.119-1G>A
XM_011545535.1:c.119-1G>A XP_011543837.1:n.119-1G>A
XM_024452390.1:c.-173-1G>A XP_024308158.1:n.-173-1G>A
XR_001755695.1:n.798-1G>A