Canonical Allele Identifier: CA412564385
Community Standard Title: NM_000444.6(PHEX):c.118+1G>T
Gene: PHEX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22033124G>T , CM000685.2:g.22033124G>T GRCh38
NC_000023.10:g.22051242G>T , CM000685.1:g.22051242G>T GRCh37
NC_000023.9:g.21961163G>T NCBI36
NG_007563.2:g.5322G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000444.6:c.118+1G>T MANE Select NP_000435.3:n.118+1G>T
ENST00000379374.5:c.118+1G>T MANE Select ENSP00000368682.4:n.118+1G>T
NM_000444.5:c.118+1G>T NP_000435.3:n.118+1G>T
NM_001282754.1:c.118+1G>T NP_001269683.1:n.118+1G>T
NM_001282754.2:c.118+1G>T NP_001269683.1:n.118+1G>T
ENST00000379374.4:c.118+1G>T ENSP00000368682.4:n.118+1G>T
ENST00000475778.2:n.544+1G>T
ENST00000683214.1:n.544+1G>T
ENST00000684143.1:c.118+1G>T ENSP00000508264.1:n.118+1G>T
XM_011545535.1:c.118+1G>T XP_011543837.1:n.118+1G>T
XR_001755695.1:n.797+1G>T