Canonical Allele Identifier: CA10368284
Gene: PHEX HGNC NCBI

Linked Data

dbSNP Id: rs748298612
gnomAD v2: X-22196428-A-C
gnomAD v4: X-22178311-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22178311A>C , CM000685.2:g.22178311A>C GRCh38
NC_000023.10:g.22196428A>C , CM000685.1:g.22196428A>C GRCh37
NC_000023.9:g.22106349A>C NCBI36
NG_007563.2:g.150508A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682888.1:c.75A>C ENSP00000508003.1:p.Leu25=
ENST00000683162.1:c.75A>C ENSP00000508059.1:p.Leu25=
ENST00000683289.1:c.75A>C ENSP00000508195.1:p.Leu25=
ENST00000683917.1:n.305A>C
ENST00000684356.1:c.75A>C ENSP00000507619.1:p.Leu25=
ENST00000684745.1:n.1195A>C
ENST00000379374.5:c.1521A>C MANE Select ENSP00000368682.4:p.Leu507=
ENST00000379374.4:c.1521A>C ENSP00000368682.4:p.Leu507=
NM_000444.5:c.1521A>C NP_000435.3:p.Leu507=
NM_001282754.1:c.1521A>C NP_001269683.1:p.Leu507=
XM_011545533.1:c.765A>C XP_011543835.1:p.Leu255=
XM_011545534.1:c.765A>C XP_011543836.1:p.Leu255=
XM_011545536.1:c.414A>C XP_011543838.1:p.Leu138=
XM_011545536.2:c.414A>C XP_011543838.1:p.Leu138=
XM_017029579.1:c.765A>C XP_016885068.1:p.Leu255=
XM_024452390.1:c.1230A>C XP_024308158.1:p.Leu410=
XR_001755695.1:n.2361A>C
NM_000444.6:c.1521A>C MANE Select NP_000435.3:p.Leu507=
NM_001282754.2:c.1521A>C NP_001269683.1:p.Leu507=