Canonical Allele Identifier: CA412574750
Gene: PHEX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22178278G>C , CM000685.2:g.22178278G>C GRCh38
NC_000023.10:g.22196395G>C , CM000685.1:g.22196395G>C GRCh37
NC_000023.9:g.22106316G>C NCBI36
NG_007563.2:g.150475G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682888.1:c.42G>C ENSP00000508003.1:p.Lys14Asn
ENST00000683162.1:c.42G>C ENSP00000508059.1:p.Lys14Asn
ENST00000683289.1:c.42G>C ENSP00000508195.1:p.Lys14Asn
ENST00000683917.1:n.272G>C
ENST00000684356.1:c.42G>C ENSP00000507619.1:p.Lys14Asn
ENST00000684745.1:n.1162G>C
ENST00000379374.5:c.1488G>C MANE Select ENSP00000368682.4:p.Lys496Asn
ENST00000379374.4:c.1488G>C ENSP00000368682.4:p.Lys496Asn
NM_000444.5:c.1488G>C NP_000435.3:p.Lys496Asn
NM_001282754.1:c.1488G>C NP_001269683.1:p.Lys496Asn
XM_011545533.1:c.732G>C XP_011543835.1:p.Lys244Asn
XM_011545534.1:c.732G>C XP_011543836.1:p.Lys244Asn
XM_011545536.1:c.381G>C XP_011543838.1:p.Lys127Asn
XM_011545536.2:c.381G>C XP_011543838.1:p.Lys127Asn
XM_017029579.1:c.732G>C XP_016885068.1:p.Lys244Asn
XM_024452390.1:c.1197G>C XP_024308158.1:p.Lys399Asn
XR_001755695.1:n.2328G>C
NM_000444.6:c.1488G>C MANE Select NP_000435.3:p.Lys496Asn
NM_001282754.2:c.1488G>C NP_001269683.1:p.Lys496Asn