Canonical Allele Identifier: CA412572721

Gene: PHEX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22097039G>T , CM000685.2:g.22097039G>T	GRCh38
NC_000023.10:g.22115157G>T , CM000685.1:g.22115157G>T	GRCh37
NC_000023.9:g.22025078G>T	NCBI36
NG_007563.2:g.69237G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000444.6:c.933+1G>T MANE Select	NP_000435.3:n.933+1G>T
ENST00000379374.5:c.933+1G>T MANE Select	ENSP00000368682.4:n.933+1G>T
NM_000444.5:c.933+1G>T	NP_000435.3:n.933+1G>T
NM_001282754.1:c.933+1G>T	NP_001269683.1:n.933+1G>T
NM_001282754.2:c.933+1G>T	NP_001269683.1:n.933+1G>T
ENST00000379374.4:c.933+1G>T	ENSP00000368682.4:n.933+1G>T
ENST00000475778.1:n.206+1G>T
ENST00000475778.2:n.1359+1G>T
ENST00000684143.1:c.930+1G>T	ENSP00000508264.1:n.930+1G>T
ENST00000684745.1:n.607+1G>T
XM_011545533.1:c.177+1G>T	XP_011543835.1:n.177+1G>T
XM_011545534.1:c.177+1G>T	XP_011543836.1:n.177+1G>T
XM_011545535.1:c.933+1G>T	XP_011543837.1:n.933+1G>T
XM_017029579.1:c.177+1G>T	XP_016885068.1:n.177+1G>T
XM_024452390.1:c.642+1G>T	XP_024308158.1:n.642+1G>T
XR_001755695.1:n.1612+1G>T