Canonical Allele Identifier: CA2419192472

Gene: PHEX PHEX-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22168390G= , CM000685.2:g.22168390G=	GRCh38
NC_000023.10:g.22186507G= , CM000685.1:g.22186507G=	GRCh37
NC_000023.9:g.22096428G=	NCBI36
NG_007563.2:g.140587G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682888.1:c.36+1G= (PHEX)	ENSP00000508003.1:n.36+1G=
ENST00000683162.1:c.36+1G= (PHEX)	ENSP00000508059.1:n.36+1G=
ENST00000683289.1:c.36+1G= (PHEX)	ENSP00000508195.1:n.36+1G=
ENST00000683917.1:n.266+1G= (PHEX)
ENST00000684356.1:c.36+1G= (PHEX)	ENSP00000507619.1:n.36+1G=
ENST00000684745.1:n.1156+1G= (PHEX)
ENST00000379374.5:c.1482+1G= (PHEX) MANE Select	ENSP00000368682.4:n.1482+1G=
ENST00000379374.4:c.1482+1G= (PHEX)	ENSP00000368682.4:n.1482+1G=
NM_000444.5:c.1482+1G= (PHEX)	NP_000435.3:n.1482+1G=
NM_001282754.1:c.1482+1G= (PHEX)	NP_001269683.1:n.1482+1G=
NR_046639.1:n.1267+1404C= (PHEX-AS1)
XM_011545533.1:c.726+1G= (PHEX)	XP_011543835.1:n.726+1G=
XM_011545534.1:c.726+1G= (PHEX)	XP_011543836.1:n.726+1G=
XM_011545536.1:c.375+1G= (PHEX)	XP_011543838.1:n.375+1G=
XM_011545536.2:c.375+1G= (PHEX)	XP_011543838.1:n.375+1G=
XM_017029579.1:c.726+1G= (PHEX)	XP_016885068.1:n.726+1G=
XM_024452390.1:c.1191+1G= (PHEX)	XP_024308158.1:n.1191+1G=
XR_001755695.1:n.2322+1G= (PHEX)
NM_000444.6:c.1482+1G= (PHEX) MANE Select	NP_000435.3:n.1482+1G=
NM_001282754.2:c.1482+1G= (PHEX)	NP_001269683.1:n.1482+1G=