Canonical Allele Identifier: CA2693304285

Gene: PHEX

Linked Data

• gnomAD v4: X-22076297-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22076297T>C , CM000685.2:g.22076297T>C	GRCh38
NC_000023.10:g.22094415T>C , CM000685.1:g.22094415T>C	GRCh37
NC_000023.9:g.22004336T>C	NCBI36
NG_007563.2:g.48495T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.776-91T>C
ENST00000683214.1:n.545-1179T>C
ENST00000684143.1:c.350-91T>C	ENSP00000508264.1:n.350-91T>C
ENST00000684745.1:n.27-91T>C
ENST00000379374.5:c.350-91T>C MANE Select	ENSP00000368682.4:n.350-91T>C
ENST00000379374.4:c.350-91T>C	ENSP00000368682.4:n.350-91T>C
NM_000444.5:c.350-91T>C	NP_000435.3:n.350-91T>C
NM_001282754.1:c.350-91T>C	NP_001269683.1:n.350-91T>C
XM_011545535.1:c.350-91T>C	XP_011543837.1:n.350-91T>C
XM_017029579.1:c.-93-14132T>C	XP_016885068.1:n.-93-14132T>C
XM_024452390.1:c.59-91T>C	XP_024308158.1:n.59-91T>C
XR_001755695.1:n.1029-91T>C
NM_000444.6:c.350-91T>C MANE Select	NP_000435.3:n.350-91T>C
NM_001282754.2:c.350-91T>C	NP_001269683.1:n.350-91T>C