Canonical Allele Identifier: CA412573389

Gene: PHEX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22114501G>A , CM000685.2:g.22114501G>A	GRCh38
NC_000023.10:g.22132619G>A , CM000685.1:g.22132619G>A	GRCh37
NC_000023.9:g.22042540G>A	NCBI36
NG_007563.2:g.86699G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000444.6:c.1217G>A MANE Select	NP_000435.3:p.Cys406Tyr
ENST00000379374.5:c.1217G>A MANE Select	ENSP00000368682.4:p.Cys406Tyr
NM_000444.5:c.1217G>A	NP_000435.3:p.Cys406Tyr
NM_001282754.1:c.1217G>A	NP_001269683.1:p.Cys406Tyr
NM_001282754.2:c.1217G>A	NP_001269683.1:p.Cys406Tyr
ENST00000379374.4:c.1217G>A	ENSP00000368682.4:p.Cys406Tyr
ENST00000684143.1:c.1214G>A	ENSP00000508264.1:p.Cys405Tyr
ENST00000684745.1:n.891G>A
XM_011545533.1:c.461G>A	XP_011543835.1:p.Cys154Tyr
XM_011545534.1:c.461G>A	XP_011543836.1:p.Cys154Tyr
XM_011545535.1:c.1217G>A	XP_011543837.1:p.Cys406Tyr
XM_011545536.1:c.110G>A	XP_011543838.1:p.Cys37Tyr
XM_011545536.2:c.110G>A	XP_011543838.1:p.Cys37Tyr
XM_017029579.1:c.461G>A	XP_016885068.1:p.Cys154Tyr
XM_024452390.1:c.926G>A	XP_024308158.1:p.Cys309Tyr
XR_001755695.1:n.1896G>A