Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22227486_22227489delinsCTCT , CM000685.2:g.22227486_22227489delinsCTCT	GRCh38
NC_000023.10:g.22245603_22245606delinsCTCT , CM000685.1:g.22245603_22245606delinsCTCT	GRCh37
NC_000023.9:g.22155524_22155527delinsCTCT	NCBI36
NG_007563.2:g.199683_199686delinsCTCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000683162.1:c.520-21_520-18delinsCTCT (PHEX)	ENSP00000508059.1:n.520-21_520-18delinsCTCT
ENST00000683289.1:c.520-21_520-18delinsCTCT (PHEX)	ENSP00000508195.1:n.520-21_520-18delinsCTCT
ENST00000683917.1:n.750-21_750-18delinsCTCT (PHEX)
ENST00000684356.1:c.520-21_520-18delinsCTCT (PHEX)	ENSP00000507619.1:n.520-21_520-18delinsCTCT
ENST00000684745.1:n.1640-21_1640-18delinsCTCT (PHEX)
ENST00000379374.5:c.1966-21_1966-18delinsCTCT (PHEX) MANE Select	ENSP00000368682.4:n.1966-21_1966-18delinsCTCT
ENST00000379374.4:c.1966-21_1966-18delinsCTCT (PHEX)	ENSP00000368682.4:n.1966-21_1966-18delinsCTCT
NM_000444.5:c.1966-21_1966-18delinsCTCT (PHEX)	NP_000435.3:n.1966-21_1966-18delinsCTCT
NM_001282754.1:c.1966-21_1966-18delinsCTCT (PHEX)	NP_001269683.1:n.1966-21_1966-18delinsCTCT
XM_011545533.1:c.1210-21_1210-18delinsCTCT (PHEX)	XP_011543835.1:n.1210-21_1210-18delinsCTCT
XM_011545534.1:c.1210-21_1210-18delinsCTCT (PHEX)	XP_011543836.1:n.1210-21_1210-18delinsCTCT
XM_011545536.1:c.859-21_859-18delinsCTCT (PHEX)	XP_011543838.1:n.859-21_859-18delinsCTCT
XR_950534.1:n.306_309delinsAGAG
NR_073010.2:n.1029_1032delinsAGAG (PTCHD1-AS)
XM_011545536.2:c.859-21_859-18delinsCTCT (PHEX)	XP_011543838.1:n.859-21_859-18delinsCTCT
XM_017029579.1:c.1210-21_1210-18delinsCTCT (PHEX)	XP_016885068.1:n.1210-21_1210-18delinsCTCT
XM_024452390.1:c.1675-21_1675-18delinsCTCT (PHEX)	XP_024308158.1:n.1675-21_1675-18delinsCTCT
XR_001755695.1:n.2806-21_2806-18delinsCTCT (PHEX)
NM_000444.6:c.1966-21_1966-18delinsCTCT (PHEX) MANE Select	NP_000435.3:n.1966-21_1966-18delinsCTCT
NM_001282754.2:c.1966-21_1966-18delinsCTCT (PHEX)	NP_001269683.1:n.1966-21_1966-18delinsCTCT