Canonical Allele Identifier: CA515423899

Gene: PHEX

Linked Data

• MyVariant Identifiers: chrX:g.22115075A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22096957A>T , CM000685.2:g.22096957A>T	GRCh38
NC_000023.10:g.22115075A>T , CM000685.1:g.22115075A>T	GRCh37
NC_000023.9:g.22024996A>T	NCBI36
NG_007563.2:g.69155A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.1278A>T
ENST00000684143.1:c.849A>T	ENSP00000508264.1:p.Ile283=
ENST00000684745.1:n.526A>T
ENST00000379374.5:c.852A>T MANE Select	ENSP00000368682.4:p.Ile284=
ENST00000379374.4:c.852A>T	ENSP00000368682.4:p.Ile284=
ENST00000475778.1:n.125A>T
NM_000444.5:c.852A>T	NP_000435.3:p.Ile284=
NM_001282754.1:c.852A>T	NP_001269683.1:p.Ile284=
XM_011545533.1:c.96A>T	XP_011543835.1:p.Ile32=
XM_011545534.1:c.96A>T	XP_011543836.1:p.Ile32=
XM_011545535.1:c.852A>T	XP_011543837.1:p.Ile284=
XM_017029579.1:c.96A>T	XP_016885068.1:p.Ile32=
XM_024452390.1:c.561A>T	XP_024308158.1:p.Ile187=
XR_001755695.1:n.1531A>T
NM_000444.6:c.852A>T MANE Select	NP_000435.3:p.Ile284=
NM_001282754.2:c.852A>T	NP_001269683.1:p.Ile284=