Canonical Allele Identifier: CA2419152316

Gene: PHEX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22046972_22046975delinsATTG , CM000685.2:g.22046972_22046975delinsATTG	GRCh38
NC_000023.10:g.22065090_22065093delinsATTG , CM000685.1:g.22065090_22065093delinsATTG	GRCh37
NC_000023.9:g.21975011_21975014delinsATTG	NCBI36
NG_007563.2:g.19170_19173delinsATTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.614-78_614-75delinsATTG
ENST00000683214.1:n.544+13849_544+13852delinsATTG
ENST00000684143.1:c.188-78_188-75delinsATTG	ENSP00000508264.1:n.188-78_188-75delinsATTG
ENST00000379374.5:c.188-78_188-75delinsATTG MANE Select	ENSP00000368682.4:n.188-78_188-75delinsATTG
ENST00000379374.4:c.188-78_188-75delinsATTG	ENSP00000368682.4:n.188-78_188-75delinsATTG
NM_000444.5:c.188-78_188-75delinsATTG	NP_000435.3:n.188-78_188-75delinsATTG
NM_001282754.1:c.188-78_188-75delinsATTG	NP_001269683.1:n.188-78_188-75delinsATTG
XM_011545535.1:c.188-78_188-75delinsATTG	XP_011543837.1:n.188-78_188-75delinsATTG
XM_024452390.1:c.-104-78_-104-75delinsATTG	XP_024308158.1:n.-104-78_-104-75delinsATTG
XR_001755695.1:n.867-78_867-75delinsATTG
NM_000444.6:c.188-78_188-75delinsATTG MANE Select	NP_000435.3:n.188-78_188-75delinsATTG
NM_001282754.2:c.188-78_188-75delinsATTG	NP_001269683.1:n.188-78_188-75delinsATTG