Canonical Allele Identifier: CA2419167650

Gene: PHEX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22094117_22094119delinsATC , CM000685.2:g.22094117_22094119delinsATC	GRCh38
NC_000023.10:g.22112235_22112237delinsATC , CM000685.1:g.22112235_22112237delinsATC	GRCh37
NC_000023.9:g.22022156_22022158delinsATC	NCBI36
NG_007563.2:g.66315_66317delinsATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.1275+18_1275+20delinsATC
ENST00000684143.1:c.846+18_846+20delinsATC	ENSP00000508264.1:n.846+18_846+20delinsATC
ENST00000684745.1:n.523+18_523+20delinsATC
ENST00000379374.5:c.849+18_849+20delinsATC MANE Select	ENSP00000368682.4:n.849+18_849+20delinsATC
ENST00000379374.4:c.849+18_849+20delinsATC	ENSP00000368682.4:n.849+18_849+20delinsATC
ENST00000475778.1:n.122+18_122+20delinsATC
NM_000444.5:c.849+18_849+20delinsATC	NP_000435.3:n.849+18_849+20delinsATC
NM_001282754.1:c.849+18_849+20delinsATC	NP_001269683.1:n.849+18_849+20delinsATC
XM_011545533.1:c.93+18_93+20delinsATC	XP_011543835.1:n.93+18_93+20delinsATC
XM_011545534.1:c.93+18_93+20delinsATC	XP_011543836.1:n.93+18_93+20delinsATC
XM_011545535.1:c.849+18_849+20delinsATC	XP_011543837.1:n.849+18_849+20delinsATC
XM_017029579.1:c.93+18_93+20delinsATC	XP_016885068.1:n.93+18_93+20delinsATC
XM_024452390.1:c.558+18_558+20delinsATC	XP_024308158.1:n.558+18_558+20delinsATC
XR_001755695.1:n.1528+18_1528+20delinsATC
NM_000444.6:c.849+18_849+20delinsATC MANE Select	NP_000435.3:n.849+18_849+20delinsATC
NM_001282754.2:c.849+18_849+20delinsATC	NP_001269683.1:n.849+18_849+20delinsATC