Canonical Allele Identifier: CA10368226

Gene: PHEX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22133594T>C , CM000685.2:g.22133594T>C	GRCh38
NC_000023.10:g.22151711T>C , CM000685.1:g.22151711T>C	GRCh37
NC_000023.9:g.22061632T>C	NCBI36
NG_007563.2:g.105791T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000444.6:c.1374T>C MANE Select	NP_000435.3:p.Asp458=
ENST00000379374.5:c.1374T>C MANE Select	ENSP00000368682.4:p.Asp458=
NM_000444.5:c.1374T>C	NP_000435.3:p.Asp458=
NM_001282754.1:c.1374T>C	NP_001269683.1:p.Asp458=
NM_001282754.2:c.1374T>C	NP_001269683.1:p.Asp458=
ENST00000379374.4:c.1374T>C	ENSP00000368682.4:p.Asp458=
ENST00000684745.1:n.1048T>C
XM_011545533.1:c.618T>C	XP_011543835.1:p.Asp206=
XM_011545534.1:c.618T>C	XP_011543836.1:p.Asp206=
XM_011545535.1:c.1374T>C	XP_011543837.1:p.Asp458=
XM_011545536.1:c.267T>C	XP_011543838.1:p.Asp89=
XM_011545536.2:c.267T>C	XP_011543838.1:p.Asp89=
XM_017029579.1:c.618T>C	XP_016885068.1:p.Asp206=
XM_024452390.1:c.1083T>C	XP_024308158.1:p.Asp361=
XR_001755695.1:n.2053T>C