Canonical Allele Identifier: CA2695231499

Gene: PHEX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22096996_22097005delinsAAACAAA , CM000685.2:g.22096996_22097005delinsAAACAAA	GRCh38
NC_000023.10:g.22115114_22115123delinsAAACAAA , CM000685.1:g.22115114_22115123delinsAAACAAA	GRCh37
NC_000023.9:g.22025035_22025044delinsAAACAAA	NCBI36
NG_007563.2:g.69194_69203delinsAAACAAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000475778.2:n.1317_1326delinsAAACAAA
ENST00000684143.1:c.888_897delinsAAACAAA	ENSP00000508264.1:p.Tyr296Ter
ENST00000684745.1:n.565_574delinsAAACAAA
ENST00000379374.5:c.891_900delinsAAACAAA MANE Select	ENSP00000368682.4:p.Tyr297Ter
ENST00000379374.4:c.891_900delinsAAACAAA	ENSP00000368682.4:p.Tyr297Ter
ENST00000475778.1:n.164_173delinsAAACAAA
NM_000444.5:c.891_900delinsAAACAAA	NP_000435.3:p.Tyr297Ter
NM_001282754.1:c.891_900delinsAAACAAA	NP_001269683.1:p.Tyr297Ter
XM_011545533.1:c.135_144delinsAAACAAA	XP_011543835.1:p.Tyr45Ter
XM_011545534.1:c.135_144delinsAAACAAA	XP_011543836.1:p.Tyr45Ter
XM_011545535.1:c.891_900delinsAAACAAA	XP_011543837.1:p.Tyr297Ter
XM_017029579.1:c.135_144delinsAAACAAA	XP_016885068.1:p.Tyr45Ter
XM_024452390.1:c.600_609delinsAAACAAA	XP_024308158.1:p.Tyr200Ter
XR_001755695.1:n.1570_1579delinsAAACAAA
NM_000444.6:c.891_900delinsAAACAAA MANE Select	NP_000435.3:p.Tyr297Ter
NM_001282754.2:c.891_900delinsAAACAAA	NP_001269683.1:p.Tyr297Ter