Canonical Allele Identifier: CA2693306111

Gene: PHEX

Linked Data

• gnomAD v4: X-22133628-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22133628A>G , CM000685.2:g.22133628A>G	GRCh38
NC_000023.10:g.22151745A>G , CM000685.1:g.22151745A>G	GRCh37
NC_000023.9:g.22061666A>G	NCBI36
NG_007563.2:g.105825A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684745.1:n.1078+4A>G
ENST00000379374.5:c.1404+4A>G MANE Select	ENSP00000368682.4:n.1404+4A>G
ENST00000379374.4:c.1404+4A>G	ENSP00000368682.4:n.1404+4A>G
NM_000444.5:c.1404+4A>G	NP_000435.3:n.1404+4A>G
NM_001282754.1:c.1404+4A>G	NP_001269683.1:n.1404+4A>G
XM_011545533.1:c.648+4A>G	XP_011543835.1:n.648+4A>G
XM_011545534.1:c.648+4A>G	XP_011543836.1:n.648+4A>G
XM_011545535.1:c.1404+4A>G	XP_011543837.1:n.1404+4A>G
XM_011545536.1:c.297+4A>G	XP_011543838.1:n.297+4A>G
XM_011545536.2:c.297+4A>G	XP_011543838.1:n.297+4A>G
XM_017029579.1:c.648+4A>G	XP_016885068.1:n.648+4A>G
XM_024452390.1:c.1113+4A>G	XP_024308158.1:n.1113+4A>G
XR_001755695.1:n.2083+4A>G
NM_000444.6:c.1404+4A>G MANE Select	NP_000435.3:n.1404+4A>G
NM_001282754.2:c.1404+4A>G	NP_001269683.1:n.1404+4A>G