Canonical Allele Identifier: CA2419168542

Gene: PHEX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22096855_22096857delinsCTT , CM000685.2:g.22096855_22096857delinsCTT	GRCh38
NC_000023.10:g.22114973_22114975delinsCTT , CM000685.1:g.22114973_22114975delinsCTT	GRCh37
NC_000023.9:g.22024894_22024896delinsCTT	NCBI36
NG_007563.2:g.69053_69055delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.1276-100_1276-98delinsCTT
ENST00000684143.1:c.847-100_847-98delinsCTT	ENSP00000508264.1:n.847-100_847-98delinsCTT
ENST00000684745.1:n.524-100_524-98delinsCTT
ENST00000379374.5:c.850-100_850-98delinsCTT MANE Select	ENSP00000368682.4:n.850-100_850-98delinsCTT
ENST00000379374.4:c.850-100_850-98delinsCTT	ENSP00000368682.4:n.850-100_850-98delinsCTT
ENST00000475778.1:n.123-100_123-98delinsCTT
NM_000444.5:c.850-100_850-98delinsCTT	NP_000435.3:n.850-100_850-98delinsCTT
NM_001282754.1:c.850-100_850-98delinsCTT	NP_001269683.1:n.850-100_850-98delinsCTT
XM_011545533.1:c.94-100_94-98delinsCTT	XP_011543835.1:n.94-100_94-98delinsCTT
XM_011545534.1:c.94-100_94-98delinsCTT	XP_011543836.1:n.94-100_94-98delinsCTT
XM_011545535.1:c.850-100_850-98delinsCTT	XP_011543837.1:n.850-100_850-98delinsCTT
XM_017029579.1:c.94-100_94-98delinsCTT	XP_016885068.1:n.94-100_94-98delinsCTT
XM_024452390.1:c.559-100_559-98delinsCTT	XP_024308158.1:n.559-100_559-98delinsCTT
XR_001755695.1:n.1529-100_1529-98delinsCTT
NM_000444.6:c.850-100_850-98delinsCTT MANE Select	NP_000435.3:n.850-100_850-98delinsCTT
NM_001282754.2:c.850-100_850-98delinsCTT	NP_001269683.1:n.850-100_850-98delinsCTT